rs121907904

Orientation

minus

Stabilized

minus

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

Make rs121907904(A;A)

Make rs121907904(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32396313

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs121907904
dbSNP (classic)	rs121907904
ClinGen	rs121907904
ebi	rs121907904
HLI	rs121907904
Exac	rs121907904
Gnomad	rs121907904
Varsome	rs121907904
LitVar	rs121907904
Map	rs121907904
PheGenI	rs121907904
Biobank	rs121907904
1000 genomes	rs121907904
hgdp	rs121907904
ensembl	rs121907904
geneview	rs121907904
scholar	rs121907904
google	rs121907904
pharmgkb	rs121907904
gwascentral	rs121907904
openSNP	rs121907904
23andMe	rs121907904
SNPshot	rs121907904
SNPdbe	rs121907904
MSV3d	rs121907904
GWAS Ctlg	rs121907904

Max Magnitude

0

OMIM	607102
Desc
Variant	0008
Related	also

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,