rs121907902

Orientation

minus

Stabilized

minus

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

Make rs121907902(A;G)

Make rs121907902(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32392013

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs121907902
dbSNP (classic)	rs121907902
ClinGen	rs121907902
ebi	rs121907902
HLI	rs121907902
Exac	rs121907902
Gnomad	rs121907902
Varsome	rs121907902
LitVar	rs121907902
Map	rs121907902
PheGenI	rs121907902
Biobank	rs121907902
1000 genomes	rs121907902
hgdp	rs121907902
ensembl	rs121907902
geneview	rs121907902
scholar	rs121907902
google	rs121907902
pharmgkb	rs121907902
gwascentral	rs121907902
openSNP	rs121907902
23andMe	rs121907902
SNPshot	rs121907902
SNPdbe	rs121907902
MSV3d	rs121907902
GWAS Ctlg	rs121907902

Max Magnitude

0

OMIM	607102
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121907902(G;G)
Alt	rs121907902(G;G)
Reference	Rs121907902(A;A)
Significance	Pathogenic
Disease	Drash syndrome
Variation	info
Gene	WT1
CLNDBN	Drash syndrome
Reversed	1
HGVS	NC_000011.9:g.32413559T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003660.2,