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rs104893882

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104893882(A;C)
Make rs104893882(C;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position6301696
GeneWFS1
is asnp
is mentioned by
dbSNPrs104893882
ebirs104893882
HLIrs104893882
Exacrs104893882
Varsomers104893882
Maprs104893882
PheGenIrs104893882
hapmaprs104893882
1000 genomesrs104893882
hgdprs104893882
ensemblrs104893882
gopubmedrs104893882
geneviewrs104893882
scholarrs104893882
googlers104893882
pharmgkbrs104893882
gwascentralrs104893882
openSNPrs104893882
23andMers104893882
23andMe allrs104893882
SNP Nexus

SNPshotrs104893882
SNPdbers104893882
MSV3drs104893882
GWAS Ctlgrs104893882
Max Magnitude0
OMIM606201
Desc
Variant0018
Relatedalso
ClinVar
Risk rs104893882(C,G;C,G)
Alt rs104893882(C,G;C,G)
Reference rs104893882(A;A)
Significance Pathogenic
Disease WFS1-Related Disorders
Variation info
Gene WFS1
CLNDBN WFS1-Related Disorders
Reversed 0
HGVS NC_000004.11:g.6303423A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004782.3,