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rs142668478

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142668478(A;A)
Make rs142668478(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position6301849
GeneWFS1
is asnp
is mentioned by
dbSNPrs142668478
ebirs142668478
HLIrs142668478
Exacrs142668478
Varsomers142668478
Maprs142668478
PheGenIrs142668478
hapmaprs142668478
1000 genomesrs142668478
hgdprs142668478
ensemblrs142668478
gopubmedrs142668478
geneviewrs142668478
scholarrs142668478
googlers142668478
pharmgkbrs142668478
gwascentralrs142668478
openSNPrs142668478
23andMers142668478
23andMe allrs142668478
SNP Nexus

SNPshotrs142668478
SNPdbers142668478
MSV3drs142668478
GWAS Ctlgrs142668478
Max Magnitude0
ClinVar
Risk rs142668478(A,C;A,C)
Alt rs142668478(A,C;A,C)
Reference rs142668478(G;G)
Significance Pathogenic
Disease not specified WFS1-Related Disorders
Variation info
Gene WFS1
CLNDBN not specified WFS1-Related Disorders
Reversed 0
HGVS NC_000004.11:g.6303576G>A; NC_000004.11:g.6303576G>C
CLNSRC ClinVar
CLNACC RCV000198254.2, RCV000038650.2,