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rs104893883

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104893883(C;C)
Make rs104893883(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position6302281
GeneWFS1
is asnp
is mentioned by
dbSNPrs104893883
ebirs104893883
HLIrs104893883
Exacrs104893883
Varsomers104893883
Maprs104893883
PheGenIrs104893883
hapmaprs104893883
1000 genomesrs104893883
hgdprs104893883
ensemblrs104893883
gopubmedrs104893883
geneviewrs104893883
scholarrs104893883
googlers104893883
pharmgkbrs104893883
gwascentralrs104893883
openSNPrs104893883
23andMers104893883
23andMe allrs104893883
SNP Nexus

SNPshotrs104893883
SNPdbers104893883
MSV3drs104893883
GWAS Ctlgrs104893883
Max Magnitude0
OMIM606201
Desc
Variant0015
Relatedalso
ClinVar
Risk rs104893883(C;C)
Alt rs104893883(C;C)
Reference rs104893883(T;T)
Significance Pathogenic
Disease WFS1-Related Disorders
Variation info
Gene WFS1
CLNDBN WFS1-Related Disorders
Reversed 0
HGVS NC_000004.11:g.6304008T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004779.3,