rs121907903

Orientation

minus

Stabilized

minus

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

Make rs121907903(C;C)

Make rs121907903(C;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32392019

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs121907903
dbSNP (classic)	rs121907903
ClinGen	rs121907903
ebi	rs121907903
HLI	rs121907903
Exac	rs121907903
Gnomad	rs121907903
Varsome	rs121907903
LitVar	rs121907903
Map	rs121907903
PheGenI	rs121907903
Biobank	rs121907903
1000 genomes	rs121907903
hgdp	rs121907903
ensembl	rs121907903
geneview	rs121907903
scholar	rs121907903
google	rs121907903
pharmgkb	rs121907903
gwascentral	rs121907903
openSNP	rs121907903
23andMe	rs121907903
SNPshot	rs121907903
SNPdbe	rs121907903
MSV3d	rs121907903
GWAS Ctlg	rs121907903

Max Magnitude

0

OMIM	607102
Desc
Variant	0007
Related	also

ClinVar
Risk	rs121907903(A;A) rs121907903(C;C)
Alt	rs121907903(A;A) rs121907903(C;C)
Reference	Rs121907903(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.32413565C>G; NC_000011.9:g.32413565C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003663.2, RCV000484903.1,