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rs762426409

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs762426409(C;T)
Make rs762426409(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position93620969
GenePDE6C
is asnp
is mentioned by
dbSNPrs762426409
ebirs762426409
HLIrs762426409
Exacrs762426409
Varsomers762426409
Maprs762426409
PheGenIrs762426409
hapmaprs762426409
1000 genomesrs762426409
hgdprs762426409
ensemblrs762426409
gopubmedrs762426409
geneviewrs762426409
scholarrs762426409
googlers762426409
pharmgkbrs762426409
gwascentralrs762426409
openSNPrs762426409
23andMers762426409
23andMe allrs762426409
SNP Nexus

SNPshotrs762426409
SNPdbers762426409
MSV3drs762426409
GWAS Ctlgrs762426409
Max Magnitude0
ClinVar
Risk rs762426409(T;T)
Alt rs762426409(T;T)
Reference rs762426409(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PDE6C
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.95380726C>T
CLNSRC
CLNACC RCV000171184.1,