Have questions? Visit https://www.reddit.com/r/SNPedia

rs113446173

From SNPedia

Orientationplus
Stabilizedplus
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
dbSNP (classic)rs113446173
ClinGenrs113446173
ebirs113446173
HLIrs113446173
Exacrs113446173
Gnomadrs113446173
Varsomers113446173
LitVarrs113446173
Maprs113446173
PheGenIrs113446173
Biobankrs113446173
1000 genomesrs113446173
hgdprs113446173
ensemblrs113446173
geneviewrs113446173
scholarrs113446173
googlers113446173
pharmgkbrs113446173
gwascentralrs113446173
openSNPrs113446173
23andMers113446173
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 UniProtKB (protein)
CLNACC RCV000488089.1,