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rs863224908

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224908(C;C)
Make rs863224908(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position93655782
GenePDE6C
is asnp
is mentioned by
dbSNPrs863224908
ebirs863224908
HLIrs863224908
Exacrs863224908
Varsomers863224908
Maprs863224908
PheGenIrs863224908
hapmaprs863224908
1000 genomesrs863224908
hgdprs863224908
ensemblrs863224908
gopubmedrs863224908
geneviewrs863224908
scholarrs863224908
googlers863224908
pharmgkbrs863224908
gwascentralrs863224908
openSNPrs863224908
23andMers863224908
23andMe allrs863224908
SNP Nexus

SNPshotrs863224908
SNPdbers863224908
MSV3drs863224908
GWAS Ctlgrs863224908
Max Magnitude0
ClinVar
Risk rs863224908(C;C)
Alt rs863224908(C;C)
Reference rs863224908(T;T)
Significance Probable-Pathogenic
Disease Cone dystrophy 4
Variation info
Gene PDE6C
CLNDBN Cone dystrophy 4
Reversed 0
HGVS NC_000010.10:g.95415539T>C
CLNSRC
CLNACC RCV000199969.1,