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rs121907901

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121907901(A;A)
Make rs121907901(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position32392704
GeneWT1
is asnp
is mentioned by
dbSNPrs121907901
ebirs121907901
HLIrs121907901
Exacrs121907901
Varsomers121907901
Maprs121907901
PheGenIrs121907901
hapmaprs121907901
1000 genomesrs121907901
hgdprs121907901
ensemblrs121907901
gopubmedrs121907901
geneviewrs121907901
scholarrs121907901
googlers121907901
pharmgkbrs121907901
gwascentralrs121907901
openSNPrs121907901
23andMers121907901
23andMe allrs121907901
SNP Nexus

SNPshotrs121907901
SNPdbers121907901
MSV3drs121907901
GWAS Ctlgrs121907901
Max Magnitude0
OMIM607102
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121907901(A;A)
Alt rs121907901(A;A)
Reference rs121907901(G;G)
Significance Pathogenic
Disease Drash syndrome
Variation info
Gene WT1
CLNDBN Drash syndrome
Reversed 1
HGVS NC_000011.9:g.32414250C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003659.3,