rs11968814

Orientation

plus

Stabilized

plus

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

Make rs11968814(A;A)

Make rs11968814(A;G)

Reference

GRCh38 38.1/141

Chromosome

6

Position

71067268

is a	snp
is	mentioned by
dbSNP	rs11968814
dbSNP (classic)	rs11968814
ClinGen	rs11968814
ebi	rs11968814
HLI	rs11968814
Exac	rs11968814
Gnomad	rs11968814
Varsome	rs11968814
LitVar	rs11968814
Map	rs11968814
PheGenI	rs11968814
Biobank	rs11968814
1000 genomes	rs11968814
hgdp	rs11968814
ensembl	rs11968814
geneview	rs11968814
scholar	rs11968814
google	rs11968814
pharmgkb	rs11968814
gwascentral	rs11968814
openSNP	rs11968814
23andMe	rs11968814
SNPshot	rs11968814
SNPdbe	rs11968814
MSV3d	rs11968814
GWAS Ctlg	rs11968814

GMAF

0.07254

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

GWAS snp
PMID	[PMID 21326311]
Trait
Title	Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients
Risk Allele	A
P-val	9E-7
Odds Ratio	1.1700 [0.70-1.64] unit decrease