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rs121907909

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121907909(C;T)
Make rs121907909(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position32392032
GeneWT1
is asnp
is mentioned by
dbSNPrs121907909
ebirs121907909
HLIrs121907909
Exacrs121907909
Varsomers121907909
Maprs121907909
PheGenIrs121907909
hapmaprs121907909
1000 genomesrs121907909
hgdprs121907909
ensemblrs121907909
gopubmedrs121907909
geneviewrs121907909
scholarrs121907909
googlers121907909
pharmgkbrs121907909
gwascentralrs121907909
openSNPrs121907909
23andMers121907909
23andMe allrs121907909
SNP Nexus

SNPshotrs121907909
SNPdbers121907909
MSV3drs121907909
GWAS Ctlgrs121907909
Max Magnitude0
OMIM607102
Desc
Variant0024
Relatedalso
ClinVar
Risk rs121907909(T;T)
Alt rs121907909(T;T)
Reference rs121907909(C;C)
Significance Pathogenic
Disease Wilms tumor 1 Frasier syndrome
Variation info
Gene WT1
CLNDBN Wilms tumor 1 Frasier syndrome
Reversed 1
HGVS NC_000011.9:g.32413578G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003666.2, RCV000030877.2,