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rs397517196

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397517196(A;C)
Make rs397517196(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position6301936
GeneWFS1
is asnp
is mentioned by
dbSNPrs397517196
ebirs397517196
HLIrs397517196
Exacrs397517196
Varsomers397517196
Maprs397517196
PheGenIrs397517196
hapmaprs397517196
1000 genomesrs397517196
hgdprs397517196
ensemblrs397517196
gopubmedrs397517196
geneviewrs397517196
scholarrs397517196
googlers397517196
pharmgkbrs397517196
gwascentralrs397517196
openSNPrs397517196
23andMers397517196
23andMe allrs397517196
SNP Nexus

SNPshotrs397517196
SNPdbers397517196
MSV3drs397517196
GWAS Ctlgrs397517196
Max Magnitude0
ClinVar
Risk rs397517196(C;C)
Alt rs397517196(C;C)
Reference rs397517196(A;A)
Significance Pathogenic
Disease WFS1-Related Disorders
Variation info
Gene WFS1
CLNDBN WFS1-Related Disorders
Reversed 0
HGVS NC_000004.11:g.6303663A>C
CLNSRC
CLNACC RCV000038651.2,