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rs121907907

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121907907(C;G)
Make rs121907907(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position32392682
GeneWT1
is asnp
is mentioned by
dbSNPrs121907907
ebirs121907907
HLIrs121907907
Exacrs121907907
Varsomers121907907
Maprs121907907
PheGenIrs121907907
hapmaprs121907907
1000 genomesrs121907907
hgdprs121907907
ensemblrs121907907
gopubmedrs121907907
geneviewrs121907907
scholarrs121907907
googlers121907907
pharmgkbrs121907907
gwascentralrs121907907
openSNPrs121907907
23andMers121907907
23andMe allrs121907907
SNP Nexus

SNPshotrs121907907
SNPdbers121907907
MSV3drs121907907
GWAS Ctlgrs121907907
Max Magnitude0
OMIM607102
Desc
Variant0015
Relatedalso
ClinVar
Risk rs121907907(G;G)
Alt rs121907907(G;G)
Reference Rs121907907(C;C)
Significance Pathogenic
Disease Drash syndrome
Variation info
Gene WT1
CLNDBN Drash syndrome
Reversed 1
HGVS NC_000011.9:g.32414228G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000003672.3,