rs121907905

Orientation

minus

Stabilized

minus

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

Make rs121907905(G;G)

Make rs121907905(G;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32392723

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs121907905
dbSNP (classic)	rs121907905
ClinGen	rs121907905
ebi	rs121907905
HLI	rs121907905
Exac	rs121907905
Gnomad	rs121907905
Varsome	rs121907905
LitVar	rs121907905
Map	rs121907905
PheGenI	rs121907905
Biobank	rs121907905
1000 genomes	rs121907905
hgdp	rs121907905
ensembl	rs121907905
geneview	rs121907905
scholar	rs121907905
google	rs121907905
pharmgkb	rs121907905
gwascentral	rs121907905
openSNP	rs121907905
23andMe	rs121907905
SNPshot	rs121907905
SNPdbe	rs121907905
MSV3d	rs121907905
GWAS Ctlg	rs121907905

Max Magnitude

0

OMIM	607102
Desc
Variant	0013
Related	also

ClinVar
Risk	rs121907905(G;G)
Alt	rs121907905(G;G)
Reference	Rs121907905(T;T)
Significance	Pathogenic
Disease	Drash syndrome
Variation	info
Gene	WT1
CLNDBN	Drash syndrome
Reversed	1
HGVS	NC_000011.9:g.32414269A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003669.3,