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rs146670741

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs146670741(A;A)
Make rs146670741(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position6301681
GeneWFS1
is asnp
is mentioned by
dbSNPrs146670741
ebirs146670741
HLIrs146670741
Exacrs146670741
Varsomers146670741
Maprs146670741
PheGenIrs146670741
hapmaprs146670741
1000 genomesrs146670741
hgdprs146670741
ensemblrs146670741
gopubmedrs146670741
geneviewrs146670741
scholarrs146670741
googlers146670741
pharmgkbrs146670741
gwascentralrs146670741
openSNPrs146670741
23andMers146670741
23andMe allrs146670741
SNP Nexus

SNPshotrs146670741
SNPdbers146670741
MSV3drs146670741
GWAS Ctlgrs146670741
Max Magnitude0
ClinVar
Risk rs146670741(A;A)
Alt rs146670741(A;A)
Reference rs146670741(G;G)
Significance Probable-Pathogenic
Disease WFS1-Related Disorders not specified
Variation info
Gene WFS1
CLNDBN WFS1-Related Disorders not specified
Reversed 0
HGVS NC_000004.11:g.6303408G>A
CLNSRC
CLNACC RCV000038647.2, RCV000196272.1,