rs35229355

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs35229355(C;T)

Make rs35229355(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

155608667

is a	snp
is	mentioned by
dbSNP	rs35229355
dbSNP (classic)	rs35229355
ClinGen	rs35229355
ebi	rs35229355
HLI	rs35229355
Exac	rs35229355
Gnomad	rs35229355
Varsome	rs35229355
LitVar	rs35229355
Map	rs35229355
PheGenI	rs35229355
Biobank	rs35229355
1000 genomes	rs35229355
hgdp	rs35229355
ensembl	rs35229355
geneview	rs35229355
scholar	rs35229355
google	rs35229355
pharmgkb	rs35229355
gwascentral	rs35229355
openSNP	rs35229355
23andMe	rs35229355
SNPshot	rs35229355
SNPdbe	rs35229355
MSV3d	rs35229355
GWAS Ctlg	rs35229355

GMAF

0.1396

Max Magnitude

0

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

GWAS snp
PMID	[PMID 19176441]
Trait	Treatment response for acute lymphoblastic leukemia
Title	Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia
Risk Allele	T
P-val	0.000005
Odds Ratio	7.24 [2.46-21.30]