Gene entry
LAMA1
laminin subunit alpha 1
- Chromosome
- 18
- Cytoband
- 18p11.31
- Variants (rsID)
- 95
LAMA1 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 18 (region 18p11.31). Its official name is “laminin subunit alpha 1”. The reference table lists 95 variants (rsID) for this gene.
Clinically classified variants
10 reference-table entries with clinical significance.
- rs12961939Benignmissense_variantPoretti-Boltshauser Syndrome
- rs566655Benignmissense_variantPoretti-Boltshauser Syndrome|Myopia|Myopia 2, Autosomal Dominant
- rs144738522Conflicting interpretationssingle nucleotide variant
- rs587777678PathogenicDeletionAtaxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome
- rs587777680PathogenicDeletionAtaxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome
- rs142934543Uncertain significancesingle nucleotide variant
- rs607230Not classifiedmissense_variantMyopia|Myopia 2, Autosomal Dominant
- rs617206Not classifiedsynonymous_variant
- rs621993Not classifiedsynonymous_variant
- rs662471Not classifiedmissense_variant
Other listed variants
- rs483480
- rs525206
- rs536173
- rs571324
- rs600134
- rs603258
- rs608532
- rs617573
- rs658121
- rs663272
- rs677136
- rs681641
- rs693754
- rs1462779
- rs2045781
- rs2045782
- rs2126566
- rs2155697
- rs2377024
- rs3810046
- rs4127404
- rs4470231
- rs4798534
- rs6506473
- rs7227276
- rs7228959
- rs7240485
- rs7243349
- rs8088532
- rs8088922
- rs8090011
- rs8095565
- rs8097469
- rs9954154
- rs11659412
- rs11664481
- rs11873205
- rs12454596
- rs12607841
- rs16951191
- rs16951199
- rs17440727
- rs17519184
- rs28369373
- rs28569884
- rs35614634
- rs62081480
- rs71360066
- rs72887927
- rs72889747
- rs74797697
- rs76073380
- rs76842111
- rs78076094
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.