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rs587776575

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587776575(A;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position32391966
GeneWT1
is asnp
is mentioned by
dbSNPrs587776575
ebirs587776575
HLIrs587776575
Exacrs587776575
Varsomers587776575
Maprs587776575
PheGenIrs587776575
hapmaprs587776575
1000 genomesrs587776575
hgdprs587776575
ensemblrs587776575
gopubmedrs587776575
geneviewrs587776575
scholarrs587776575
googlers587776575
pharmgkbrs587776575
gwascentralrs587776575
openSNPrs587776575
23andMers587776575
23andMe allrs587776575
SNP Nexus

SNPshotrs587776575
SNPdbers587776575
MSV3drs587776575
GWAS Ctlgrs587776575
Max Magnitude0
ClinVar
Risk rs587776575(A;A)
Alt rs587776575(A;A)
Reference rs587776575(T;T)
Significance Pathogenic
Disease Frasier syndrome
Variation info
Gene WT1
CLNDBN Frasier syndrome
Reversed 1
HGVS NC_000011.9:g.32413512A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003655.2,