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rs587776574

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(GT;GT) 0 common in clinvar
Make rs587776574(-;-)
Make rs587776574(-;C)
ReferenceGRCh38 38.1/142
Chromosome11
Position32399967
GeneWT1
is asnp
is mentioned by
dbSNPrs587776574
ebirs587776574
HLIrs587776574
Exacrs587776574
Varsomers587776574
Maprs587776574
PheGenIrs587776574
hapmaprs587776574
1000 genomesrs587776574
hgdprs587776574
ensemblrs587776574
gopubmedrs587776574
geneviewrs587776574
scholarrs587776574
googlers587776574
pharmgkbrs587776574
gwascentralrs587776574
openSNPrs587776574
23andMers587776574
23andMe allrs587776574
SNP Nexus

SNPshotrs587776574
SNPdbers587776574
MSV3drs587776574
GWAS Ctlgrs587776574
Max Magnitude0
ClinVar
Risk rs587776574(CT,T;CT,T)
Alt rs587776574(CT,T;CT,T)
Reference rs587776574(GT;GT)
Significance Pathogenic
Disease Wilms tumor 1
Variation info
Gene WT1
CLNDBN Wilms tumor 1
Reversed 1
HGVS NC_000011.9:g.32421513delC
CLNSRC OMIM Allelic Variant
CLNACC RCV000003654.2,