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rs121907906

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121907906(C;T)
Make rs121907906(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position32392717
GeneWT1
is asnp
is mentioned by
dbSNPrs121907906
ebirs121907906
HLIrs121907906
Exacrs121907906
Varsomers121907906
Maprs121907906
PheGenIrs121907906
hapmaprs121907906
1000 genomesrs121907906
hgdprs121907906
ensemblrs121907906
gopubmedrs121907906
geneviewrs121907906
scholarrs121907906
googlers121907906
pharmgkbrs121907906
gwascentralrs121907906
openSNPrs121907906
23andMers121907906
23andMe allrs121907906
SNP Nexus

SNPshotrs121907906
SNPdbers121907906
MSV3drs121907906
GWAS Ctlgrs121907906
Max Magnitude0
OMIM607102
Desc
Variant0014
Relatedalso
ClinVar
Risk rs121907906(T;T)
Alt rs121907906(T;T)
Reference rs121907906(C;C)
Significance Pathogenic
Disease Drash syndrome Wilms tumor 1
Variation info
Gene WT1
CLNDBN Drash syndrome Wilms tumor 1
Reversed 1
HGVS NC_000011.9:g.32414263G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003670.2, RCV000003671.2,