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rs267606691

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606691(A;A)
Make rs267606691(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position29073706
GeneC2orf71
is asnp
is mentioned by
dbSNPrs267606691
ebirs267606691
HLIrs267606691
Exacrs267606691
Varsomers267606691
Maprs267606691
PheGenIrs267606691
hapmaprs267606691
1000 genomesrs267606691
hgdprs267606691
ensemblrs267606691
gopubmedrs267606691
geneviewrs267606691
scholarrs267606691
googlers267606691
pharmgkbrs267606691
gwascentralrs267606691
openSNPrs267606691
23andMers267606691
23andMe allrs267606691
SNP Nexus

SNPshotrs267606691
SNPdbers267606691
MSV3drs267606691
GWAS Ctlgrs267606691
Max Magnitude0
ClinVar
Risk rs267606691(A,G,T;A,G,T)
Alt rs267606691(A,G,T;A,G,T)
Reference rs267606691(C;C)
Significance Pathogenic
Disease Retinitis pigmentosa 54
Variation info
Gene C2orf71
CLNDBN Retinitis pigmentosa 54
Reversed 1
HGVS NC_000002.11:g.29296572G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000000124.3,