rs776155094

Orientation

plus

Stabilized

plus

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

Make rs776155094(-;-)

Make rs776155094(-;C)

Reference

GRCh38.p7 38.3/149

Chromosome

11

Position

32435210

Gene	WT1, WT1-AS

is a	snp
is	mentioned by
dbSNP	rs776155094
dbSNP (classic)	rs776155094
ClinGen	rs776155094
ebi	rs776155094
HLI	rs776155094
Exac	rs776155094
Gnomad	rs776155094
Varsome	rs776155094
LitVar	rs776155094
Map	rs776155094
PheGenI	rs776155094
Biobank	rs776155094
1000 genomes	rs776155094
hgdp	rs776155094
ensembl	rs776155094
geneview	rs776155094
scholar	rs776155094
google	rs776155094
pharmgkb	rs776155094
gwascentral	rs776155094
openSNP	rs776155094
23andMe	rs776155094
SNPshot	rs776155094
SNPdbe	rs776155094
MSV3d	rs776155094
GWAS Ctlg	rs776155094

Max Magnitude

0

ClinVar
Risk	rs776155094(-;-)
Alt	rs776155094(-;-)
Reference	Rs776155094(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	WT1 WT1-AS
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.32456756delC
CLNSRC
CLNACC	RCV000255852.1,