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rs28937892

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs28937892(C;T)
Make rs28937892(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position6301306
GeneWFS1
is asnp
is mentioned by
dbSNPrs28937892
ebirs28937892
HLIrs28937892
Exacrs28937892
Varsomers28937892
Maprs28937892
PheGenIrs28937892
hapmaprs28937892
1000 genomesrs28937892
hgdprs28937892
ensemblrs28937892
gopubmedrs28937892
geneviewrs28937892
scholarrs28937892
googlers28937892
pharmgkbrs28937892
gwascentralrs28937892
openSNPrs28937892
23andMers28937892
23andMe allrs28937892
SNP Nexus

SNPshotrs28937892
SNPdbers28937892
MSV3drs28937892
GWAS Ctlgrs28937892
Max Magnitude0
OMIM606201
DescWOLFRAM SYNDROME
Variant0006
Relatedalso
Neighborrs28937891
Distance573
Neighborrs1801212
Distance514
Neighborrs734312
Distance321


ClinVar
Risk rs28937892(T;T)
Alt rs28937892(T;T)
Reference rs28937892(C;C)
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.6303033C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004770.3,