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rs869025561

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869025561(G;T)
Make rs869025561(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome11
Position32392755
GeneWT1
is asnp
is mentioned by
dbSNPrs869025561
ebirs869025561
HLIrs869025561
Exacrs869025561
Varsomers869025561
Maprs869025561
PheGenIrs869025561
hapmaprs869025561
1000 genomesrs869025561
hgdprs869025561
ensemblrs869025561
gopubmedrs869025561
geneviewrs869025561
scholarrs869025561
googlers869025561
pharmgkbrs869025561
gwascentralrs869025561
openSNPrs869025561
23andMers869025561
23andMe allrs869025561
SNP Nexus

SNPshotrs869025561
SNPdbers869025561
MSV3drs869025561
GWAS Ctlgrs869025561
Max Magnitude0
ClinVar
Risk rs869025561(T;T)
Alt rs869025561(T;T)
Reference rs869025561(G;G)
Significance Probable-Pathogenic
Disease Hereditary nephrotic syndrome
Variation info
Gene WT1
CLNDBN Hereditary nephrotic syndrome
Reversed 1
HGVS NC_000011.9:g.32414301C>A
CLNSRC
CLNACC RCV000208133.1,