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rs121907910

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121907910(C;T)
Make rs121907910(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position32392705
GeneWT1
is asnp
is mentioned by
dbSNPrs121907910
ebirs121907910
HLIrs121907910
Exacrs121907910
Varsomers121907910
Maprs121907910
PheGenIrs121907910
hapmaprs121907910
1000 genomesrs121907910
hgdprs121907910
ensemblrs121907910
gopubmedrs121907910
geneviewrs121907910
scholarrs121907910
googlers121907910
pharmgkbrs121907910
gwascentralrs121907910
openSNPrs121907910
23andMers121907910
23andMe allrs121907910
SNP Nexus

SNPshotrs121907910
SNPdbers121907910
MSV3drs121907910
GWAS Ctlgrs121907910
Max Magnitude0
OMIM607102
Desc
Variant0026
Relatedalso
ClinVar
Risk rs121907910(T;T)
Alt rs121907910(T;T)
Reference rs121907910(C;C)
Significance Pathogenic
Disease Meacham syndrome
Variation info
Gene WT1
CLNDBN Meacham syndrome
Reversed 1
HGVS NC_000011.9:g.32414251G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003680.2,