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rs121907905

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121907905(G;G)
Make rs121907905(G;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position32392723
GeneWT1
is asnp
is mentioned by
dbSNPrs121907905
ebirs121907905
HLIrs121907905
Exacrs121907905
Varsomers121907905
Maprs121907905
PheGenIrs121907905
hapmaprs121907905
1000 genomesrs121907905
hgdprs121907905
ensemblrs121907905
gopubmedrs121907905
geneviewrs121907905
scholarrs121907905
googlers121907905
pharmgkbrs121907905
gwascentralrs121907905
openSNPrs121907905
23andMers121907905
23andMe allrs121907905
SNP Nexus

SNPshotrs121907905
SNPdbers121907905
MSV3drs121907905
GWAS Ctlgrs121907905
Max Magnitude0
OMIM607102
Desc
Variant0013
Relatedalso
ClinVar
Risk rs121907905(G;G)
Alt rs121907905(G;G)
Reference rs121907905(T;T)
Significance Pathogenic
Disease Drash syndrome
Variation info
Gene WT1
CLNDBN Drash syndrome
Reversed 1
HGVS NC_000011.9:g.32414269A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003669.2,