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rs121907911

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121907911(A;A)
Make rs121907911(A;C)
ReferenceGRCh38 38.1/141
Chromosome11
Position32434815
GeneWT1, WT1-AS
is asnp
is mentioned by
dbSNPrs121907911
ebirs121907911
HLIrs121907911
Exacrs121907911
Varsomers121907911
Maprs121907911
PheGenIrs121907911
hapmaprs121907911
1000 genomesrs121907911
hgdprs121907911
ensemblrs121907911
gopubmedrs121907911
geneviewrs121907911
scholarrs121907911
googlers121907911
pharmgkbrs121907911
gwascentralrs121907911
openSNPrs121907911
23andMers121907911
23andMe allrs121907911
SNP Nexus

SNPshotrs121907911
SNPdbers121907911
MSV3drs121907911
GWAS Ctlgrs121907911
Max Magnitude0
OMIM607102
Desc
Variant0027
Relatedalso
ClinVar
Risk rs121907911(A;A)
Alt rs121907911(A;A)
Reference rs121907911(C;C)
Significance Pathogenic
Disease Wilms tumor 1
Variation info
Gene WT1 WT1-AS
CLNDBN Wilms tumor 1
Reversed 1
HGVS NC_000011.9:g.32456361G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003681.2,