rs121907907

Orientation

minus

Stabilized

minus

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

Make rs121907907(C;G)

Make rs121907907(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32392682

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs121907907
dbSNP (classic)	rs121907907
ClinGen	rs121907907
ebi	rs121907907
HLI	rs121907907
Exac	rs121907907
Gnomad	rs121907907
Varsome	rs121907907
LitVar	rs121907907
Map	rs121907907
PheGenI	rs121907907
Biobank	rs121907907
1000 genomes	rs121907907
hgdp	rs121907907
ensembl	rs121907907
geneview	rs121907907
scholar	rs121907907
google	rs121907907
pharmgkb	rs121907907
gwascentral	rs121907907
openSNP	rs121907907
23andMe	rs121907907
SNPshot	rs121907907
SNPdbe	rs121907907
MSV3d	rs121907907
GWAS Ctlg	rs121907907

Max Magnitude

0

OMIM	607102
Desc
Variant	0015
Related	also

ClinVar
Risk	rs121907907(G;G)
Alt	rs121907907(G;G)
Reference	Rs121907907(C;C)
Significance	Pathogenic
Disease	Drash syndrome
Variation	info
Gene	WT1
CLNDBN	Drash syndrome
Reversed	1
HGVS	NC_000011.9:g.32414228G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003672.3,