Have questions? Visit https://www.reddit.com/r/SNPedia

rs56002719

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs56002719(A;T)
Make rs56002719(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome4
Position6302122
GeneWFS1
is asnp
is mentioned by
dbSNPrs56002719
dbSNP (old)rs56002719
ClinGenrs56002719
ebirs56002719
HLIrs56002719
Exacrs56002719
Gnomadrs56002719
Varsomers56002719
Maprs56002719
PheGenIrs56002719
Biobankrs56002719
1000 genomesrs56002719
hgdprs56002719
ensemblrs56002719
gopubmedrs56002719
geneviewrs56002719
scholarrs56002719
googlers56002719
pharmgkbrs56002719
gwascentralrs56002719
openSNPrs56002719
23andMers56002719
23andMe allrs56002719
SNP Nexus

SNPshotrs56002719
SNPdbers56002719
MSV3drs56002719
GWAS Ctlgrs56002719
Max Magnitude0
ClinVar
Risk rs56002719(T;T)
Alt rs56002719(T;T)
Reference Rs56002719(A;A)
Significance Other
Disease not specified WFS1-Related Spectrum Disorders
Variation info
Gene WFS1
CLNDBN not specified WFS1-Related Spectrum Disorders
Reversed 0
HGVS NC_000004.11:g.6303849A>T
CLNSRC
CLNACC RCV000152695.3, RCV000351538.1,