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rs121907903

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121907903(C;C)
Make rs121907903(C;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position32392019
GeneWT1
is asnp
is mentioned by
dbSNPrs121907903
ebirs121907903
HLIrs121907903
Exacrs121907903
Varsomers121907903
Maprs121907903
PheGenIrs121907903
hapmaprs121907903
1000 genomesrs121907903
hgdprs121907903
ensemblrs121907903
gopubmedrs121907903
geneviewrs121907903
scholarrs121907903
googlers121907903
pharmgkbrs121907903
gwascentralrs121907903
openSNPrs121907903
23andMers121907903
23andMe allrs121907903
SNP Nexus

SNPshotrs121907903
SNPdbers121907903
MSV3drs121907903
GWAS Ctlgrs121907903
Max Magnitude0
OMIM607102
Desc
Variant0007
Relatedalso
ClinVar
Risk rs121907903(C;C)
Alt rs121907903(C;C)
Reference rs121907903(G;G)
Significance Pathogenic
Disease Drash syndrome
Variation info
Gene WT1
CLNDBN Drash syndrome
Reversed 1
HGVS NC_000011.9:g.32413565C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000003663.2,