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

rs786205462

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205462(C;C)
Make rs786205462(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position93640200
GenePDE6C
is asnp
is mentioned by
dbSNPrs786205462
ebirs786205462
HLIrs786205462
Exacrs786205462
Varsomers786205462
Maprs786205462
PheGenIrs786205462
hapmaprs786205462
1000 genomesrs786205462
hgdprs786205462
ensemblrs786205462
gopubmedrs786205462
geneviewrs786205462
scholarrs786205462
googlers786205462
pharmgkbrs786205462
gwascentralrs786205462
openSNPrs786205462
23andMers786205462
23andMe allrs786205462
SNP Nexus

SNPshotrs786205462
SNPdbers786205462
MSV3drs786205462
GWAS Ctlgrs786205462
Max Magnitude0
ClinVar
Risk rs786205462(C;C)
Alt rs786205462(C;C)
Reference rs786205462(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PDE6C
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.95399957T>C
CLNSRC
CLNACC RCV000171186.1,