rs121907910

Orientation

minus

Stabilized

minus

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

Make rs121907910(C;T)

Make rs121907910(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32392705

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs121907910
dbSNP (classic)	rs121907910
ClinGen	rs121907910
ebi	rs121907910
HLI	rs121907910
Exac	rs121907910
Gnomad	rs121907910
Varsome	rs121907910
LitVar	rs121907910
Map	rs121907910
PheGenI	rs121907910
Biobank	rs121907910
1000 genomes	rs121907910
hgdp	rs121907910
ensembl	rs121907910
geneview	rs121907910
scholar	rs121907910
google	rs121907910
pharmgkb	rs121907910
gwascentral	rs121907910
openSNP	rs121907910
23andMe	rs121907910
SNPshot	rs121907910
SNPdbe	rs121907910
MSV3d	rs121907910
GWAS Ctlg	rs121907910

Max Magnitude

0

OMIM	607102
Desc
Variant	0026
Related	also

ClinVar
Risk	rs121907910(T;T)
Alt	rs121907910(T;T)
Reference	Rs121907910(C;C)
Significance	Pathogenic
Disease	Meacham syndrome
Variation	info
Gene	WT1
CLNDBN	Meacham syndrome
Reversed	1
HGVS	NC_000011.9:g.32414251G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003680.3,