rs2213169

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common genotype

Make rs2213169(C;T)

Make rs2213169(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

5281833

is a	snp
is	mentioned by
dbSNP	rs2213169
dbSNP (classic)	rs2213169
ClinGen	rs2213169
ebi	rs2213169
HLI	rs2213169
Exac	rs2213169
Gnomad	rs2213169
Varsome	rs2213169
LitVar	rs2213169
Map	rs2213169
PheGenI	rs2213169
Biobank	rs2213169
1000 genomes	rs2213169
hgdp	rs2213169
ensembl	rs2213169
geneview	rs2213169
scholar	rs2213169
google	rs2213169
pharmgkb	rs2213169
gwascentral	rs2213169
openSNP	rs2213169
23andMe	rs2213169
SNPshot	rs2213169
SNPdbe	rs2213169
MSV3d	rs2213169
GWAS Ctlg	rs2213169

GMAF

0.04316

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23263863]
Trait	Hematology traits
Title	GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children.
Risk Allele	T
P-val	5E-11
Odds Ratio	.45 [0.31-0.58] unit decrease