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rs587776576

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776576(C;T)
Make rs587776576(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position32391967
GeneWT1
is asnp
is mentioned by
dbSNPrs587776576
ebirs587776576
HLIrs587776576
Exacrs587776576
Varsomers587776576
Maprs587776576
PheGenIrs587776576
hapmaprs587776576
1000 genomesrs587776576
hgdprs587776576
ensemblrs587776576
gopubmedrs587776576
geneviewrs587776576
scholarrs587776576
googlers587776576
pharmgkbrs587776576
gwascentralrs587776576
openSNPrs587776576
23andMers587776576
23andMe allrs587776576
SNP Nexus

SNPshotrs587776576
SNPdbers587776576
MSV3drs587776576
GWAS Ctlgrs587776576
Max Magnitude0
ClinVar
Risk rs587776576(C,T;C,T)
Alt rs587776576(C,T;C,T)
Reference rs587776576(G;G)
Significance Pathogenic
Disease Drash syndrome Frasier syndrome Hereditary nephrotic syndrome
Variation info
Gene WT1
CLNDBN Drash syndrome Frasier syndrome Hereditary nephrotic syndrome
Reversed 1
HGVS NC_000011.9:g.32413513C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003665.2, RCV000030876.2, RCV000208283.1,