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rs267606936

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs267606936(A;A)
Make rs267606936(A;G)
ReferenceGRCh38 38.1/141
Chromosome10
Position93663028
GenePDE6C
is asnp
is mentioned by
dbSNPrs267606936
ebirs267606936
HLIrs267606936
Exacrs267606936
Varsomers267606936
Maprs267606936
PheGenIrs267606936
hapmaprs267606936
1000 genomesrs267606936
hgdprs267606936
ensemblrs267606936
gopubmedrs267606936
geneviewrs267606936
scholarrs267606936
googlers267606936
pharmgkbrs267606936
gwascentralrs267606936
openSNPrs267606936
23andMers267606936
23andMe allrs267606936
SNP Nexus

SNPshotrs267606936
SNPdbers267606936
MSV3drs267606936
GWAS Ctlgrs267606936
Max Magnitude0
ClinVar
Risk rs267606936(A;A)
Alt rs267606936(A;A)
Reference rs267606936(G;G)
Significance Pathogenic
Disease Achromatopsia 5
Variation info
Gene PDE6C
CLNDBN Achromatopsia 5
Reversed 0
HGVS NC_000010.10:g.95422785G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009314.4,