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rs121907904

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121907904(A;A)
Make rs121907904(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position32396313
GeneWT1
is asnp
is mentioned by
dbSNPrs121907904
ebirs121907904
HLIrs121907904
Exacrs121907904
Varsomers121907904
Maprs121907904
PheGenIrs121907904
hapmaprs121907904
1000 genomesrs121907904
hgdprs121907904
ensemblrs121907904
gopubmedrs121907904
geneviewrs121907904
scholarrs121907904
googlers121907904
pharmgkbrs121907904
gwascentralrs121907904
openSNPrs121907904
23andMers121907904
23andMe allrs121907904
SNP Nexus

SNPshotrs121907904
SNPdbers121907904
MSV3drs121907904
GWAS Ctlgrs121907904
Max Magnitude0
OMIM607102
Desc
Variant0008
Relatedalso
ClinVar
Risk rs121907904(A;A)
Alt rs121907904(A;A)
Reference rs121907904(G;G)
Significance Pathogenic
Disease Drash syndrome
Variation info
Gene WT1
CLNDBN Drash syndrome
Reversed 1
HGVS NC_000011.9:g.32417859C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000003664.2,