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

rs104893880

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893880(C;T)
Make rs104893880(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position6291961
GeneWFS1
is asnp
is mentioned by
dbSNPrs104893880
ebirs104893880
HLIrs104893880
Exacrs104893880
Varsomers104893880
Maprs104893880
PheGenIrs104893880
hapmaprs104893880
1000 genomesrs104893880
hgdprs104893880
ensemblrs104893880
gopubmedrs104893880
geneviewrs104893880
scholarrs104893880
googlers104893880
pharmgkbrs104893880
gwascentralrs104893880
openSNPrs104893880
23andMers104893880
23andMe allrs104893880
SNP Nexus

SNPshotrs104893880
SNPdbers104893880
MSV3drs104893880
GWAS Ctlgrs104893880
Max Magnitude0
OMIM606201
Desc
Variant0010
Relatedalso
ClinVar
Risk rs104893880(T;T)
Alt rs104893880(T;T)
Reference rs104893880(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.6293688C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004774.5,