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rs56393026

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs56393026(A;A)
Make rs56393026(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6302398
GeneWFS1
is asnp
is mentioned by
dbSNPrs56393026
ebirs56393026
HLIrs56393026
Exacrs56393026
Varsomers56393026
Maprs56393026
PheGenIrs56393026
hapmaprs56393026
1000 genomesrs56393026
hgdprs56393026
ensemblrs56393026
gopubmedrs56393026
geneviewrs56393026
scholarrs56393026
googlers56393026
pharmgkbrs56393026
gwascentralrs56393026
openSNPrs56393026
23andMers56393026
23andMe allrs56393026
SNP Nexus

SNPshotrs56393026
SNPdbers56393026
MSV3drs56393026
GWAS Ctlgrs56393026
Max Magnitude0
ClinVar
Risk rs56393026(A;A)
Alt rs56393026(A;A)
Reference rs56393026(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6304125G>A
CLNSRC
CLNACC RCV000199675.1,