rs121907908

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in complete genomics
(A;G)	7.5	Wilms tumor susceptibility (predicted)

Make rs121907908(G;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

32400025

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs121907908
dbSNP (classic)	rs121907908
ClinGen	rs121907908
ebi	rs121907908
HLI	rs121907908
Exac	rs121907908
Gnomad	rs121907908
Varsome	rs121907908
LitVar	rs121907908
Map	rs121907908
PheGenI	rs121907908
Biobank	rs121907908
1000 genomes	rs121907908
hgdp	rs121907908
ensembl	rs121907908
geneview	rs121907908
scholar	rs121907908
google	rs121907908
pharmgkb	rs121907908
gwascentral	rs121907908
openSNP	rs121907908
23andMe	rs121907908
SNPshot	rs121907908
SNPdbe	rs121907908
MSV3d	rs121907908
GWAS Ctlg	rs121907908

Max Magnitude

7.5

aka c.1021A>G (p.Ser341Gly)

OMIM	607102
Desc
Variant	0016
Related	also

ClinVar
Risk	rs121907908(G;G)
Alt	rs121907908(G;G)
Reference	Rs121907908(A;A)
Significance	Pathogenic
Disease	Mesothelioma
Variation	info
Gene	WT1
CLNDBN	Mesothelioma
Reversed	1
HGVS	NC_000011.9:g.32421571T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003673.4,