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rs267606794

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606794(C;T)
Make rs267606794(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position61840319
GeneFAM161A
is asnp
is mentioned by
dbSNPrs267606794
ebirs267606794
HLIrs267606794
Exacrs267606794
Varsomers267606794
Maprs267606794
PheGenIrs267606794
hapmaprs267606794
1000 genomesrs267606794
hgdprs267606794
ensemblrs267606794
gopubmedrs267606794
geneviewrs267606794
scholarrs267606794
googlers267606794
pharmgkbrs267606794
gwascentralrs267606794
openSNPrs267606794
23andMers267606794
23andMe allrs267606794
SNP Nexus

SNPshotrs267606794
SNPdbers267606794
MSV3drs267606794
GWAS Ctlgrs267606794
Max Magnitude0
ClinVar
Risk rs267606794(T;T)
Alt rs267606794(T;T)
Reference rs267606794(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 28
Variation info
Gene FAM161A
CLNDBN Retinitis pigmentosa 28
Reversed 1
HGVS NC_000002.11:g.62067454G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000052.2,