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rs387906930

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906930(C;T)
Make rs387906930(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position6301846
GeneWFS1
is asnp
is mentioned by
dbSNPrs387906930
ebirs387906930
HLIrs387906930
Exacrs387906930
Varsomers387906930
Maprs387906930
PheGenIrs387906930
hapmaprs387906930
1000 genomesrs387906930
hgdprs387906930
ensemblrs387906930
gopubmedrs387906930
geneviewrs387906930
scholarrs387906930
googlers387906930
pharmgkbrs387906930
gwascentralrs387906930
openSNPrs387906930
23andMers387906930
23andMe allrs387906930
SNP Nexus

SNPshotrs387906930
SNPdbers387906930
MSV3drs387906930
GWAS Ctlgrs387906930
Max Magnitude0
ClinVar
Risk rs387906930(T;T)
Alt rs387906930(T;T)
Reference rs387906930(C;C)
Significance Pathogenic
Disease Wolfram-like syndrome Diabetes mellitus AND insipidus with optic atrophy AND deafness not provided
Variation info
Gene WFS1
CLNDBN Wolfram-like syndrome, autosomal dominant Diabetes mellitus AND insipidus with optic atrophy AND deafness not provided
Reversed 0
HGVS NC_000004.11:g.6303573C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000023514.4, RCV000023515.4, RCV000200668.1,