rs587776575

Orientation

plus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(T;T)	0	common in clinvar

Make rs587776575(A;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

32391966

Gene

WT1

is a	snp
is	mentioned by
dbSNP	rs587776575
dbSNP (classic)	rs587776575
ClinGen	rs587776575
ebi	rs587776575
HLI	rs587776575
Exac	rs587776575
Gnomad	rs587776575
Varsome	rs587776575
LitVar	rs587776575
Map	rs587776575
PheGenI	rs587776575
Biobank	rs587776575
1000 genomes	rs587776575
hgdp	rs587776575
ensembl	rs587776575
geneview	rs587776575
scholar	rs587776575
google	rs587776575
pharmgkb	rs587776575
gwascentral	rs587776575
openSNP	rs587776575
23andMe	rs587776575
SNPshot	rs587776575
SNPdbe	rs587776575
MSV3d	rs587776575
GWAS Ctlg	rs587776575

Max Magnitude

0

ClinVar
Risk	Rs587776575(A;A)
Alt	Rs587776575(A;A)
Reference	Rs587776575(T;T)
Significance	Pathogenic
Disease	Frasier syndrome
Variation	info
Gene	WT1
CLNDBN	Frasier syndrome
Reversed	1
HGVS	NC_000011.9:g.32413512A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000003655.2,