rs587776573

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(-;ATTTATACCAAATGACA)	7.5	Wilms tumor susceptibility (predicted)
(-;TGTCATTTGGTATAAAT)	7.5	Wilms tumor susceptibility (predicted)
(ATTTATACCAAATGACA;ATTTATACCAAATGACA)	0	common in clinvar
(ATTTATACCAAATGACAT;ATTTATACCAAATGACAT)	0	common in clinvar
(TGTCATTTGGTATAAAT;TGTCATTTGGTATAAAT)	0	common in clinvar

Make rs587776573(-;-)

Reference

GRCh38 38.1/142

Chromosome

11

Position

32417633

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs587776573
dbSNP (classic)	rs587776573
ClinGen	rs587776573
ebi	rs587776573
HLI	rs587776573
Exac	rs587776573
Gnomad	rs587776573
Varsome	rs587776573
LitVar	rs587776573
Map	rs587776573
PheGenI	rs587776573
Biobank	rs587776573
1000 genomes	rs587776573
hgdp	rs587776573
ensembl	rs587776573
geneview	rs587776573
scholar	rs587776573
google	rs587776573
pharmgkb	rs587776573
gwascentral	rs587776573
openSNP	rs587776573
23andMe	rs587776573
SNPshot	rs587776573
SNPdbe	rs587776573
MSV3d	rs587776573
GWAS Ctlg	rs587776573

Max Magnitude

7.5

aka c.242_258del17 (p.Asn81Ilefs)

ClinVar
Risk	Rs587776573(TGTCATTTGGTATAAAT;TGTCATTTGGTATAAAT) rs587776573(-;-)
Alt	Rs587776573(TGTCATTTGGTATAAAT;TGTCATTTGGTATAAAT) rs587776573(-;-)
Reference	Rs587776573(ATTTATACCAAATGACA;ATTTATACCAAATGACA)
Significance	Pathogenic
Disease	Wilms tumor 1
Variation	info
Gene	WT1
CLNDBN	Wilms tumor 1
Reversed	1
HGVS	NC_000011.9:g.32439179_32439195del17
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003653.2,