Gene entry
RELN
reelin
- Chromosome
- 7
- Cytoband
- 7q22.1
- Variants (rsID)
- 183
RELN is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7q22.1). Its official name is “reelin”. The reference table lists 183 variants (rsID) for this gene.
Clinically classified variants
44 reference-table entries with clinical significance.
- rs113242008Benignsingle nucleotide variantFamilial temporal lobe epilepsy 7|Norman-Roberts syndrome|Norman-Roberts syndrome
- rs114003896Benignsingle nucleotide variantNorman-Roberts syndrome|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7
- rs114019779Benignsingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs114684479Benignsingle nucleotide variantChildhood epilepsy with centrotemporal spikes|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs115379833Benignsingle nucleotide variantNorman-Roberts syndrome|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7
- rs115734214Benignsingle nucleotide variantNorman-Roberts syndrome|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7
- rs116716038Benignsingle nucleotide variantNorman-Roberts syndrome|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7|Intellectual disability
- rs13232021Benignsingle nucleotide variant
- rs2711866Benignsingle nucleotide variantNorman-Roberts syndrome|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7
- rs3025962Benignsingle nucleotide variantChildhood epilepsy with centrotemporal spikes|Norman-Roberts syndrome|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7
- rs362726Benignsingle nucleotide variantNorman-Roberts syndrome
- rs362746Benignsingle nucleotide variantNorman-Roberts syndrome|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7
- rs41276148Benignsingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs55689103Benignsingle nucleotide variantFamilial temporal lobe epilepsy 7|Norman-Roberts syndrome|Norman-Roberts syndrome
- rs74513461Benignsingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs77664442Benignsingle nucleotide variantNorman-Roberts syndrome|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7
- rs78008536Benignsingle nucleotide variantFamilial temporal lobe epilepsy 7|Norman-Roberts syndrome|Norman-Roberts syndrome
- rs79610081Benignsingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs114344654Conflicting interpretationssingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs114501042Conflicting interpretationssingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs114807343Conflicting interpretationssingle nucleotide variantFamilial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs115035120Conflicting interpretationssingle nucleotide variantChildhood epilepsy with centrotemporal spikes|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7
- rs116065504Conflicting interpretationssingle nucleotide variantFamilial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs143050366Conflicting interpretationssingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Epilepsy, familial temporal lobe, 1|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7|Intellectual disability
- rs143213152Conflicting interpretationssingle nucleotide variantFamilial temporal lobe epilepsy 7|Norman-Roberts syndrome|Norman-Roberts syndrome
- rs150236371Conflicting interpretationssingle nucleotide variantFamilial temporal lobe epilepsy 7|Norman-Roberts syndrome|Norman-Roberts syndrome|Intellectual disability
- rs2229860Conflicting interpretationssingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs41275239Conflicting interpretationssingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs542352292Conflicting interpretationssingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs55693709Conflicting interpretationssingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs56342240Conflicting interpretationssingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs78480723Conflicting interpretationssingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs79161241Conflicting interpretationssingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs188371196Likely benignsingle nucleotide variantFamilial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs115549751Uncertain significancesingle nucleotide variantFamilial temporal lobe epilepsy 7|Norman-Roberts syndrome|Norman-Roberts syndrome
- rs116463039Uncertain significancesingle nucleotide variantNorman-Roberts syndrome|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7
- rs116634494Uncertain significancesingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome|Intellectual disability
- rs138909076Uncertain significancesingle nucleotide variantFamilial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs143948239Uncertain significancesingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7
- rs185075003Uncertain significancesingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7
- rs188328812Uncertain significancesingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7
- rs200007424Uncertain significancesingle nucleotide variantNorman-Roberts syndrome|Familial temporal lobe epilepsy 7
- rs201788015Uncertain significancesingle nucleotide variantFamilial temporal lobe epilepsy 7|Norman-Roberts syndrome
- rs56146903Uncertain significancesingle nucleotide variantFamilial temporal lobe epilepsy 7|Norman-Roberts syndrome|Familial temporal lobe epilepsy 7|Norman-Roberts syndrome|Epilepsy, familial temporal lobe, 1|Norman-Roberts syndrome
Other listed variants
- rs39326
- rs39335
- rs39351
- rs144525
- rs362635
- rs362642
- rs362698
- rs362710
- rs362719
- rs362780
- rs362790
- rs362794
- rs362806
- rs471360
- rs492063
- rs496907
- rs528528
- rs540058
- rs649365
- rs727708
- rs736707
- rs745541
- rs802786
- rs802788
- rs876425
- rs917716
- rs1705107
- rs2075040
- rs2075044
- rs2159676
- rs2159677
- rs2191703
- rs2237628
- rs2256517
- rs2256670
- rs2283021
- rs2299351
- rs2299356
- rs2299381
- rs2299402
- rs2528858
- rs2528865
- rs2535757
- rs2711870
- rs2711878
- rs3808040
- rs3808048
- rs3808050
- rs3819466
- rs3823992
- rs3857816
- rs3898845
- rs3914125
- rs3914126
- rs3914132
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.