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rs1801208

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1801208(A;A)
Make rs1801208(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position6301162
GeneWFS1
is asnp
is mentioned by
dbSNPrs1801208
ebirs1801208
HLIrs1801208
Exacrs1801208
Varsomers1801208
Maprs1801208
PheGenIrs1801208
hapmaprs1801208
1000 genomesrs1801208
hgdprs1801208
ensemblrs1801208
gopubmedrs1801208
geneviewrs1801208
scholarrs1801208
googlers1801208
pharmgkbrs1801208
gwascentralrs1801208
openSNPrs1801208
23andMers1801208
23andMe allrs1801208
SNP Nexus

SNPshotrs1801208
SNPdbers1801208
MSV3drs1801208
GWAS Ctlgrs1801208
GMAF0.05556
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 19258739] Association study of the effect of WFS1 polymorphisms on risk of type 2 diabetes in Japanese population


GET Evidence
WFS1-R456H
aa_change Arg456His
aa_change_short R456H
impact not reviewed
qualified_impact Insufficiently evaluated not reviewed
overall_frequency 0.0454545
summary



ClinVar
Risk rs1801208(A;A)
Alt rs1801208(A;A)
Reference rs1801208(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene WFS1
CLNDBN not specified
Reversed 0
HGVS NC_000004.11:g.6302889G>A
CLNSRC HGMD
CLNACC RCV000038638.7,