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rs587776577

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587776577(A;A)
Make rs587776577(A;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position32391968
GeneWT1
is asnp
is mentioned by
dbSNPrs587776577
ebirs587776577
HLIrs587776577
Exacrs587776577
Varsomers587776577
Maprs587776577
PheGenIrs587776577
hapmaprs587776577
1000 genomesrs587776577
hgdprs587776577
ensemblrs587776577
gopubmedrs587776577
geneviewrs587776577
scholarrs587776577
googlers587776577
pharmgkbrs587776577
gwascentralrs587776577
openSNPrs587776577
23andMers587776577
23andMe allrs587776577
SNP Nexus

SNPshotrs587776577
SNPdbers587776577
MSV3drs587776577
GWAS Ctlgrs587776577
Max Magnitude0
ClinVar
Risk rs587776577(A,G;A,G)
Alt rs587776577(A,G;A,G)
Reference rs587776577(C;C)
Significance Pathogenic
Disease Frasier syndrome Diffuse mesangial sclerosis Hereditary nephrotic syndrome
Variation info
Gene WT1
CLNDBN Frasier syndrome Diffuse mesangial sclerosis Hereditary nephrotic syndrome
Reversed 1
HGVS NC_000011.9:g.32413514G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003674.2, RCV000003675.2, RCV000157584.1,