Gene entry
ADGRV1
adhesion G protein-coupled receptor V1
- Chromosome
- 5
- Cytoband
- 5q14.3
- Variants (rsID)
- 171
ADGRV1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 5 (region 5q14.3). Its official name is “adhesion G protein-coupled receptor V1”. The reference table lists 171 variants (rsID) for this gene.
Clinically classified variants
90 reference-table entries with clinical significance.
- rs10037067Benignsingle nucleotide variantUsher syndrome type 2C
- rs111033429Benignsingle nucleotide variantUsher syndrome type 2C
- rs111033430Benignsingle nucleotide variantUsher syndrome type 2C
- rs111033530Benignsingle nucleotide variantUsher syndrome type 2C
- rs111753827Benignsingle nucleotide variant
- rs13158963Benignsingle nucleotide variantUsher syndrome type 2C
- rs142013761Benignsingle nucleotide variant
- rs145294917Benignsingle nucleotide variant
- rs146120983Benignsingle nucleotide variant
- rs147062294Benignsingle nucleotide variantUsher syndrome type 2C
- rs149390094Benignsingle nucleotide variantUsher syndrome type 2C
- rs16868972Benignsingle nucleotide variantUsher syndrome type 2C
- rs16868974Benignsingle nucleotide variantUsher syndrome type 2C
- rs16869032Benignsingle nucleotide variantUsher syndrome type 2C
- rs17544552Benignsingle nucleotide variantUsher syndrome type 2C
- rs17624033Benignsingle nucleotide variantUsher syndrome type 2C
- rs1878878Benignsingle nucleotide variantUsher syndrome type 2C
- rs200055351Benignsingle nucleotide variantUsher syndrome type 2C
- rs2366777Benignsingle nucleotide variantUsher syndrome type 2C
- rs2366926Benignsingle nucleotide variantUsher syndrome type 2C
- rs2366928Benignsingle nucleotide variantUsher syndrome type 2C
- rs3763073Benignsingle nucleotide variantUsher syndrome type 2C
- rs41304884Benignsingle nucleotide variantUsher syndrome type 2C
- rs41311333Benignsingle nucleotide variantUsher syndrome type 2C
- rs4916684Benignsingle nucleotide variantUsher syndrome type 2C
- rs4916685Benignsingle nucleotide variantUsher syndrome type 2C
- rs61731030Benignsingle nucleotide variantUsher syndrome type 2C
- rs61745498Benignsingle nucleotide variantUsher syndrome type 2C
- rs6889939Benignsingle nucleotide variantUsher syndrome type 2C
- rs74632023Benignsingle nucleotide variant
- rs950692Benignsingle nucleotide variantUsher syndrome type 2C
- rs111033517Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs113498662Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs115239207Conflicting interpretationssingle nucleotide variant
- rs13171868Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs137853918Conflicting interpretationssingle nucleotide variantFebrile seizures, familial, 4|Usher syndrome type 2C
- rs138908576Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C|Febrile seizures, familial, 4|Usher syndrome type 2C
- rs144918959Conflicting interpretationssingle nucleotide variant
- rs145556097Conflicting interpretationssingle nucleotide variantFebrile seizures, familial, 4|Usher syndrome type 2C
- rs146954342Conflicting interpretationssingle nucleotide variant
- rs148097083Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs181146384Conflicting interpretationssingle nucleotide variant
- rs182395524Conflicting interpretationssingle nucleotide variantFebrile seizures, familial, 4
- rs182990046Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs183319660Conflicting interpretationssingle nucleotide variant
- rs183633457Conflicting interpretationssingle nucleotide variantFebrile seizures, familial, 4|Usher syndrome type 2C|Usher syndrome type 2C
- rs188772875Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C|Febrile seizures, familial, 4|Usher syndrome type 2C
- rs189967386Conflicting interpretationssingle nucleotide variant
- rs190922596Conflicting interpretationssingle nucleotide variantFebrile seizures, familial, 4|Usher syndrome type 2C
- rs193030567Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs199587998Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C|Retinitis pigmentosa
- rs199988872Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs200392821Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs200816323Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C|Febrile seizures, familial, 4|Usher syndrome type 2C|Hearing impairment
- rs201236317Conflicting interpretationssingle nucleotide variant
- rs201386977Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs201481219Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs201890097Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs201963060Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs202064612Conflicting interpretationssingle nucleotide variantFebrile seizures, familial, 4|Usher syndrome type 2C|Seizure
- rs202066007Conflicting interpretationssingle nucleotide variant
- rs202106463Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs202190568Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs202211640Conflicting interpretationssingle nucleotide variant
- rs369083434Conflicting interpretationssingle nucleotide variant
- rs371947306Conflicting interpretationssingle nucleotide variantUsher syndrome type 1|Usher syndrome type 2C
- rs373352597Conflicting interpretationssingle nucleotide variant
- rs373354231Conflicting interpretationssingle nucleotide variant
- rs375062187Conflicting interpretationssingle nucleotide variant
- rs375921325Conflicting interpretationssingle nucleotide variant
- rs397517442Conflicting interpretationssingle nucleotide variant
- rs41302834Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs41305898Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs41308297Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs41308846Conflicting interpretationssingle nucleotide variantFebrile seizures, familial, 4|Usher syndrome type 2C
- rs41311335Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs56329646Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs61744480Conflicting interpretationssingle nucleotide variantUsher syndrome type 2C
- rs200106260Likely benignsingle nucleotide variant
- rs121909762Pathogenicsingle nucleotide variantUsher syndrome type 2C|Usher syndrome|Febrile seizures, familial, 4|Usher syndrome type 2C|Rare genetic deafness
- rs371981035Pathogenicsingle nucleotide variantRare genetic deafness|Retinal dystrophy|Usher syndrome type 2
- rs373780305Pathogenicsingle nucleotide variantRare genetic deafness|Usher syndrome type 2C|Febrile seizures, familial, 4
- rs376689763Pathogenicsingle nucleotide variantRare genetic deafness
- rs141681122Uncertain significancesingle nucleotide variant
- rs146526977Uncertain significancesingle nucleotide variantUsher syndrome type 2C
- rs182698253Uncertain significancesingle nucleotide variantFebrile seizures, familial, 4|Usher syndrome type 2C|Usher syndrome type 2C
- rs186975400Uncertain significancesingle nucleotide variant
- rs200197273Uncertain significancesingle nucleotide variantUsher syndrome type 2C
- rs200644004Uncertain significancesingle nucleotide variantFebrile seizures, familial, 4|Usher syndrome type 2C|Usher syndrome type 2C
- rs201747452Uncertain significancesingle nucleotide variantUsher syndrome type 2C
Other listed variants
- rs168743
- rs1967256
- rs1995776
- rs2222244
- rs2366771
- rs2366935
- rs2438361
- rs2460167
- rs2697542
- rs2973442
- rs2973447
- rs3105792
- rs4244206
- rs4916845
- rs4916848
- rs6864534
- rs6879563
- rs7706034
- rs7711918
- rs7721198
- rs7727492
- rs7730204
- rs7732169
- rs10038122
- rs10062423
- rs10068613
- rs10070771
- rs10213801
- rs10514341
- rs10514345
- rs11956622
- rs12517229
- rs16869285
- rs16869392
- rs16869414
- rs17553041
- rs17613704
- rs34088804
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.