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rs767561828

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs767561828(G;G)
Make rs767561828(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6300990
GeneWFS1
is asnp
is mentioned by
dbSNPrs767561828
dbSNP (old)rs767561828
ClinGenrs767561828
ebirs767561828
HLIrs767561828
Exacrs767561828
Gnomadrs767561828
Varsomers767561828
Maprs767561828
PheGenIrs767561828
Biobankrs767561828
1000 genomesrs767561828
hgdprs767561828
ensemblrs767561828
gopubmedrs767561828
geneviewrs767561828
scholarrs767561828
googlers767561828
pharmgkbrs767561828
gwascentralrs767561828
openSNPrs767561828
23andMers767561828
23andMe allrs767561828
SNP Nexus

SNPshotrs767561828
SNPdbers767561828
MSV3drs767561828
GWAS Ctlgrs767561828
Max Magnitude0
ClinVar
Risk rs767561828(G;G)
Alt rs767561828(G;G)
Reference Rs767561828(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene WFS1
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.6302717T>G
CLNSRC
CLNACC RCV000195821.2,