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rs28937891

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs28937891(G;T)
Make rs28937891(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position6301879
GeneWFS1
is asnp
is mentioned by
dbSNPrs28937891
ebirs28937891
HLIrs28937891
Exacrs28937891
Varsomers28937891
Maprs28937891
PheGenIrs28937891
hapmaprs28937891
1000 genomesrs28937891
hgdprs28937891
ensemblrs28937891
gopubmedrs28937891
geneviewrs28937891
scholarrs28937891
googlers28937891
pharmgkbrs28937891
gwascentralrs28937891
openSNPrs28937891
23andMers28937891
23andMe allrs28937891
SNP Nexus

SNPshotrs28937891
SNPdbers28937891
MSV3drs28937891
GWAS Ctlgrs28937891
Max Magnitude0
OMIM606201
DescWOLFRAM SYNDROME
Variant0004
Relatedalso
Neighborrs28937892
Distance573
Neighborrs28937894
Distance12


ClinVar
Risk rs28937891(A,T;A,T)
Alt rs28937891(A,T;A,T)
Reference rs28937891(G;G)
Significance Pathogenic
Disease Diabetes mellitus AND insipidus with optic atrophy AND deafness
Variation info
Gene WFS1
CLNDBN Diabetes mellitus AND insipidus with optic atrophy AND deafness
Reversed 0
HGVS NC_000004.11:g.6303606G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004768.5,