rs121907901

Orientation

minus

Stabilized

minus

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

Make rs121907901(A;A)

Make rs121907901(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32392704

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs121907901
dbSNP (classic)	rs121907901
ClinGen	rs121907901
ebi	rs121907901
HLI	rs121907901
Exac	rs121907901
Gnomad	rs121907901
Varsome	rs121907901
LitVar	rs121907901
Map	rs121907901
PheGenI	rs121907901
Biobank	rs121907901
1000 genomes	rs121907901
hgdp	rs121907901
ensembl	rs121907901
geneview	rs121907901
scholar	rs121907901
google	rs121907901
pharmgkb	rs121907901
gwascentral	rs121907901
openSNP	rs121907901
23andMe	rs121907901
SNPshot	rs121907901
SNPdbe	rs121907901
MSV3d	rs121907901
GWAS Ctlg	rs121907901

Max Magnitude

0

OMIM	607102
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121907901(A;A)
Alt	rs121907901(A;A)
Reference	Rs121907901(G;G)
Significance	Pathogenic
Disease	Drash syndrome not provided
Variation	info
Gene	WT1
CLNDBN	Drash syndrome not provided
Reversed	1
HGVS	NC_000011.9:g.32414250C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003659.3, RCV000484493.1,