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rs786205463

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs786205463(C;C)
Make rs786205463(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position93655770
GenePDE6C
is asnp
is mentioned by
dbSNPrs786205463
ebirs786205463
HLIrs786205463
Exacrs786205463
Varsomers786205463
Maprs786205463
PheGenIrs786205463
hapmaprs786205463
1000 genomesrs786205463
hgdprs786205463
ensemblrs786205463
gopubmedrs786205463
geneviewrs786205463
scholarrs786205463
googlers786205463
pharmgkbrs786205463
gwascentralrs786205463
openSNPrs786205463
23andMers786205463
23andMe allrs786205463
SNP Nexus

SNPshotrs786205463
SNPdbers786205463
MSV3drs786205463
GWAS Ctlgrs786205463
Max Magnitude0
ClinVar
Risk rs786205463(C;C)
Alt rs786205463(C;C)
Reference rs786205463(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PDE6C
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.95415527T>C
CLNSRC
CLNACC RCV000171187.1,