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rs121907900

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121907900(C;T)
Make rs121907900(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position32392020
GeneWT1
is asnp
is mentioned by
dbSNPrs121907900
ebirs121907900
HLIrs121907900
Exacrs121907900
Varsomers121907900
Maprs121907900
PheGenIrs121907900
hapmaprs121907900
1000 genomesrs121907900
hgdprs121907900
ensemblrs121907900
gopubmedrs121907900
geneviewrs121907900
scholarrs121907900
googlers121907900
pharmgkbrs121907900
gwascentralrs121907900
openSNPrs121907900
23andMers121907900
23andMe allrs121907900
SNP Nexus

SNPshotrs121907900
SNPdbers121907900
MSV3drs121907900
GWAS Ctlgrs121907900
Max Magnitude0
OMIM607102
Desc
Variant0003
Relatedalso
ClinVar
Risk rs121907900(T;T)
Alt rs121907900(T;T)
Reference rs121907900(C;C)
Significance Pathogenic
Disease Drash syndrome Meacham syndrome Diffuse mesangial sclerosis
Variation info
Gene WT1
CLNDBN Drash syndrome Meacham syndrome Diffuse mesangial sclerosis
Reversed 1
HGVS NC_000011.9:g.32413566G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000003656.2, RCV000003657.2, RCV000003658.2,