rs1496766

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common genotype

Make rs1496766(C;C)

Make rs1496766(C;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

78702149

Gene

MAGI2

is a	snp
is	mentioned by
dbSNP	rs1496766
dbSNP (classic)	rs1496766
ClinGen	rs1496766
ebi	rs1496766
HLI	rs1496766
Exac	rs1496766
Gnomad	rs1496766
Varsome	rs1496766
LitVar	rs1496766
Map	rs1496766
PheGenI	rs1496766
Biobank	rs1496766
1000 genomes	rs1496766
hgdp	rs1496766
ensembl	rs1496766
geneview	rs1496766
scholar	rs1496766
google	rs1496766
pharmgkb	rs1496766
gwascentral	rs1496766
openSNP	rs1496766
23andMe	rs1496766
SNPshot	rs1496766
SNPdbe	rs1496766
MSV3d	rs1496766
GWAS Ctlg	rs1496766

GMAF

0.03949

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 23007406]
Trait	Acute lymphoblastic leukemia (childhood)
Title	Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.
Risk Allele	C
P-val	5E-6
Odds Ratio	2.84 [1.81-4.44]