Have questions? Visit https://www.reddit.com/r/SNPedia

rs267606876

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606876(C;T)
Make rs267606876(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position101243615
GeneIMPG2
is asnp
is mentioned by
dbSNPrs267606876
ebirs267606876
HLIrs267606876
Exacrs267606876
Varsomers267606876
Maprs267606876
PheGenIrs267606876
hapmaprs267606876
1000 genomesrs267606876
hgdprs267606876
ensemblrs267606876
gopubmedrs267606876
geneviewrs267606876
scholarrs267606876
googlers267606876
pharmgkbrs267606876
gwascentralrs267606876
openSNPrs267606876
23andMers267606876
23andMe allrs267606876
SNP Nexus

SNPshotrs267606876
SNPdbers267606876
MSV3drs267606876
GWAS Ctlgrs267606876
Max Magnitude0
ClinVar
Risk rs267606876(T;T)
Alt rs267606876(T;T)
Reference rs267606876(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 56
Variation info
Gene IMPG2
CLNDBN Retinitis pigmentosa 56
Reversed 1
HGVS NC_000003.11:g.100962459G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003726.2,