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

rs267606937

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267606937(C;T)
Make rs267606937(T;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position93622034
GenePDE6C
is asnp
is mentioned by
dbSNPrs267606937
ebirs267606937
HLIrs267606937
Exacrs267606937
Varsomers267606937
Maprs267606937
PheGenIrs267606937
hapmaprs267606937
1000 genomesrs267606937
hgdprs267606937
ensemblrs267606937
gopubmedrs267606937
geneviewrs267606937
scholarrs267606937
googlers267606937
pharmgkbrs267606937
gwascentralrs267606937
openSNPrs267606937
23andMers267606937
23andMe allrs267606937
SNP Nexus

SNPshotrs267606937
SNPdbers267606937
MSV3drs267606937
GWAS Ctlgrs267606937
Max Magnitude0
ClinVar
Risk rs267606937(T;T)
Alt rs267606937(T;T)
Reference rs267606937(C;C)
Significance Pathogenic
Disease Achromatopsia 5
Variation info
Gene PDE6C
CLNDBN Achromatopsia 5
Reversed 0
HGVS NC_000010.10:g.95381791C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009318.4,