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

rs267606935

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs267606935(A;A)
Make rs267606935(A;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position93663117
GenePDE6C
is asnp
is mentioned by
dbSNPrs267606935
ebirs267606935
HLIrs267606935
Exacrs267606935
Varsomers267606935
Maprs267606935
PheGenIrs267606935
hapmaprs267606935
1000 genomesrs267606935
hgdprs267606935
ensemblrs267606935
gopubmedrs267606935
geneviewrs267606935
scholarrs267606935
googlers267606935
pharmgkbrs267606935
gwascentralrs267606935
openSNPrs267606935
23andMers267606935
23andMe allrs267606935
SNP Nexus

SNPshotrs267606935
SNPdbers267606935
MSV3drs267606935
GWAS Ctlgrs267606935
Max Magnitude0
ClinVar
Risk rs267606935(A;A)
Alt rs267606935(A;A)
Reference rs267606935(T;T)
Significance Pathogenic
Disease Achromatopsia 5
Variation info
Gene PDE6C
CLNDBN Achromatopsia 5
Reversed 0
HGVS NC_000010.10:g.95422874T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009319.3,