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rs797045075

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045075(C;C)
Make rs797045075(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6302058
GeneWFS1
is asnp
is mentioned by
dbSNPrs797045075
ebirs797045075
HLIrs797045075
Exacrs797045075
Varsomers797045075
Maprs797045075
PheGenIrs797045075
hapmaprs797045075
1000 genomesrs797045075
hgdprs797045075
ensemblrs797045075
gopubmedrs797045075
geneviewrs797045075
scholarrs797045075
googlers797045075
pharmgkbrs797045075
gwascentralrs797045075
openSNPrs797045075
23andMers797045075
23andMe allrs797045075
SNP Nexus

SNPshotrs797045075
SNPdbers797045075
MSV3drs797045075
GWAS Ctlgrs797045075
Max Magnitude0
ClinVar
Risk rs797045075(C;C)
Alt rs797045075(C;C)
Reference rs797045075(T;T)
Significance Probable-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.6303785T>C
CLNSRC Baylor College of Medicine
CLNACC RCV000191145.1,