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rs121907908

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs121907908(A;G)
Make rs121907908(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position32400025
GeneWT1
is asnp
is mentioned by
dbSNPrs121907908
ebirs121907908
HLIrs121907908
Exacrs121907908
Varsomers121907908
Maprs121907908
PheGenIrs121907908
hapmaprs121907908
1000 genomesrs121907908
hgdprs121907908
ensemblrs121907908
gopubmedrs121907908
geneviewrs121907908
scholarrs121907908
googlers121907908
pharmgkbrs121907908
gwascentralrs121907908
openSNPrs121907908
23andMers121907908
23andMe allrs121907908
SNP Nexus

SNPshotrs121907908
SNPdbers121907908
MSV3drs121907908
GWAS Ctlgrs121907908
Max Magnitude0
OMIM607102
Desc
Variant0016
Relatedalso
ClinVar
Risk rs121907908(G;G)
Alt rs121907908(G;G)
Reference rs121907908(A;A)
Significance Pathogenic
Disease Mesothelioma
Variation info
Gene WT1
CLNDBN Mesothelioma
Reversed 1
HGVS NC_000011.9:g.32421571T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003673.4,