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rs863224262

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs863224262(G;G)
Make rs863224262(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6302377
GeneWFS1
is asnp
is mentioned by
dbSNPrs863224262
ebirs863224262
HLIrs863224262
Exacrs863224262
Varsomers863224262
Maprs863224262
PheGenIrs863224262
hapmaprs863224262
1000 genomesrs863224262
hgdprs863224262
ensemblrs863224262
gopubmedrs863224262
geneviewrs863224262
scholarrs863224262
googlers863224262
pharmgkbrs863224262
gwascentralrs863224262
openSNPrs863224262
23andMers863224262
23andMe allrs863224262
SNP Nexus

SNPshotrs863224262
SNPdbers863224262
MSV3drs863224262
GWAS Ctlgrs863224262
Max Magnitude0
ClinVar
Risk rs863224262(G;G)
Alt rs863224262(G;G)
Reference rs863224262(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6304104T>G
CLNSRC
CLNACC RCV000197483.1,