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rs777580652

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs777580652(C;T)
Make rs777580652(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6300668
GeneWFS1
is asnp
is mentioned by
dbSNPrs777580652
ebirs777580652
HLIrs777580652
Exacrs777580652
Varsomers777580652
Maprs777580652
PheGenIrs777580652
hapmaprs777580652
1000 genomesrs777580652
hgdprs777580652
ensemblrs777580652
gopubmedrs777580652
geneviewrs777580652
scholarrs777580652
googlers777580652
pharmgkbrs777580652
gwascentralrs777580652
openSNPrs777580652
23andMers777580652
23andMe allrs777580652
SNP Nexus

SNPshotrs777580652
SNPdbers777580652
MSV3drs777580652
GWAS Ctlgrs777580652
Max Magnitude0
ClinVar
Risk rs777580652(T;T)
Alt rs777580652(T;T)
Reference rs777580652(C;C)
Significance Pathogenic
Disease Wolfram syndrome
Variation info
Gene WFS1
CLNDBN Wolfram syndrome
Reversed 0
HGVS NC_000004.11:g.6302395C>G
CLNSRC
CLNACC RCV000192573.1,