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rs1799925

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1799925(C;T)
Make rs1799925(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position32435016
GeneWT1, WT1-AS
is asnp
is mentioned by
dbSNPrs1799925
ebirs1799925
HLIrs1799925
Exacrs1799925
Varsomers1799925
Maprs1799925
PheGenIrs1799925
hapmaprs1799925
1000 genomesrs1799925
hgdprs1799925
ensemblrs1799925
gopubmedrs1799925
geneviewrs1799925
scholarrs1799925
googlers1799925
pharmgkbrs1799925
gwascentralrs1799925
openSNPrs1799925
23andMers1799925
23andMe allrs1799925
SNP Nexus

SNPshotrs1799925
SNPdbers1799925
MSV3drs1799925
GWAS Ctlgrs1799925
GMAF0.3154
Max Magnitude0

[PMID 23484026OA-icon.png] Single Nucleotide Polymorphisms in the Wilms' Tumour Gene 1 in Clear Cell Renal Cell Carcinoma

ClinVar
Risk rs1799925(T;T)
Alt rs1799925(T;T)
Reference rs1799925(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene WT1 WT1-AS
CLNDBN not specified
Reversed 1
HGVS NC_000011.9:g.32456562G>A
CLNSRC
CLNACC RCV000173525.1,