rs41322152

Orientation

plus

Stabilized

plus

Make rs41322152(C;C)

Make rs41322152(C;G)

Make rs41322152(G;G)

Reference

GRCh38 38.1/142

Chromosome

10

Position

70281049

Gene

NPFFR1

is a	snp
is	mentioned by
dbSNP	rs41322152
dbSNP (classic)	rs41322152
ClinGen	rs41322152
ebi	rs41322152
HLI	rs41322152
Exac	rs41322152
Gnomad	rs41322152
Varsome	rs41322152
LitVar	rs41322152
Map	rs41322152
PheGenI	rs41322152
Biobank	rs41322152
1000 genomes	rs41322152
hgdp	rs41322152
ensembl	rs41322152
geneview	rs41322152
scholar	rs41322152
google	rs41322152
pharmgkb	rs41322152
gwascentral	rs41322152
openSNP	rs41322152
23andMe	rs41322152
SNPshot	rs41322152
SNPdbe	rs41322152
MSV3d	rs41322152
GWAS Ctlg	rs41322152

GMAF

0.02479

Max Magnitude

0

?	(C;C) (C;G) (G;G)	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	8E-6
Odds Ratio	2.52 [1.68-3.79]