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rs113446173

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs113446173(G;T)
Make rs113446173(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6301166
GeneWFS1
is asnp
is mentioned by
dbSNPrs113446173
ebirs113446173
HLIrs113446173
Exacrs113446173
Varsomers113446173
Maprs113446173
PheGenIrs113446173
hapmaprs113446173
1000 genomesrs113446173
hgdprs113446173
ensemblrs113446173
gopubmedrs113446173
geneviewrs113446173
scholarrs113446173
googlers113446173
pharmgkbrs113446173
gwascentralrs113446173
openSNPrs113446173
23andMers113446173
23andMe allrs113446173
SNP Nexus

SNPshotrs113446173
SNPdbers113446173
MSV3drs113446173
GWAS Ctlgrs113446173
Max Magnitude0
ClinVar
Risk rs113446173(T;T)
Alt rs113446173(T;T)
Reference rs113446173(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6302893G>T
CLNSRC
CLNACC RCV000195642.1,