rs1799925

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1799925(C;T)

Make rs1799925(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32435016

Gene	WT1, WT1-AS

is a	snp
is	mentioned by
dbSNP	rs1799925
dbSNP (classic)	rs1799925
ClinGen	rs1799925
ebi	rs1799925
HLI	rs1799925
Exac	rs1799925
Gnomad	rs1799925
Varsome	rs1799925
LitVar	rs1799925
Map	rs1799925
PheGenI	rs1799925
Biobank	rs1799925
1000 genomes	rs1799925
hgdp	rs1799925
ensembl	rs1799925
geneview	rs1799925
scholar	rs1799925
google	rs1799925
pharmgkb	rs1799925
gwascentral	rs1799925
openSNP	rs1799925
23andMe	rs1799925
SNPshot	rs1799925
SNPdbe	rs1799925
MSV3d	rs1799925
GWAS Ctlg	rs1799925

GMAF

0.3154

Max Magnitude

0

[PMID 23484026] 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 Wilms tumor Diffuse mesangial sclerosis Wilms Tumor Meacham syndrome
Variation	info
Gene	WT1 WT1-AS
CLNDBN	not specified Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome Diffuse mesangial sclerosis Wilms Tumor Meacham syndrome
Reversed	1
HGVS	NC_000011.9:g.32456562G>A
CLNSRC
CLNACC	RCV000173525.3, RCV000268679.1, RCV000309796.1, RCV000363346.1, RCV000364660.1,