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rs121907902

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121907902(A;G)
Make rs121907902(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position32392013
GeneWT1
is asnp
is mentioned by
dbSNPrs121907902
ebirs121907902
HLIrs121907902
Exacrs121907902
Varsomers121907902
Maprs121907902
PheGenIrs121907902
hapmaprs121907902
1000 genomesrs121907902
hgdprs121907902
ensemblrs121907902
gopubmedrs121907902
geneviewrs121907902
scholarrs121907902
googlers121907902
pharmgkbrs121907902
gwascentralrs121907902
openSNPrs121907902
23andMers121907902
23andMe allrs121907902
SNP Nexus

SNPshotrs121907902
SNPdbers121907902
MSV3drs121907902
GWAS Ctlgrs121907902
Max Magnitude0
OMIM607102
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121907902(G;G)
Alt rs121907902(G;G)
Reference rs121907902(A;A)
Significance Pathogenic
Disease Drash syndrome
Variation info
Gene WT1
CLNDBN Drash syndrome
Reversed 1
HGVS NC_000011.9:g.32413559T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003660.2,