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rs104893881

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893881(C;T)
Make rs104893881(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position6302250
GeneWFS1
is asnp
is mentioned by
dbSNPrs104893881
ebirs104893881
HLIrs104893881
Exacrs104893881
Varsomers104893881
Maprs104893881
PheGenIrs104893881
hapmaprs104893881
1000 genomesrs104893881
hgdprs104893881
ensemblrs104893881
gopubmedrs104893881
geneviewrs104893881
scholarrs104893881
googlers104893881
pharmgkbrs104893881
gwascentralrs104893881
openSNPrs104893881
23andMers104893881
23andMe allrs104893881
SNP Nexus

SNPshotrs104893881
SNPdbers104893881
MSV3drs104893881
GWAS Ctlgrs104893881
Max Magnitude0
OMIM606201
Desc
Variant0011
Relatedalso
ClinVar
Risk rs104893881(T;T)
Alt rs104893881(T;T)
Reference rs104893881(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.6303977C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000004775.5,