rs11065987

Orientation

plus

Stabilized

plus

Make rs11065987(A;A)

Make rs11065987(A;G)

Make rs11065987(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

111634620

is a	snp
is	mentioned by
dbSNP	rs11065987
dbSNP (classic)	rs11065987
ClinGen	rs11065987
ebi	rs11065987
HLI	rs11065987
Exac	rs11065987
Gnomad	rs11065987
Varsome	rs11065987
LitVar	rs11065987
Map	rs11065987
PheGenI	rs11065987
Biobank	rs11065987
1000 genomes	rs11065987
hgdp	rs11065987
ensembl	rs11065987
geneview	rs11065987
scholar	rs11065987
google	rs11065987
pharmgkb	rs11065987
gwascentral	rs11065987
openSNP	rs11065987
23andMe	rs11065987
SNPshot	rs11065987
SNPdbe	rs11065987
MSV3d	rs11065987
GWAS Ctlg	rs11065987

GMAF

0.1965

Max Magnitude

0

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

GWAS snp
PMID	[PMID 19862010]
Trait	Hematocrit
Title	Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium
Risk Allele	G
P-val	1E-12
Odds Ratio	0.17 [0.12-0.22] % decrease

GWAS snp
PMID	[PMID 20686565]
Trait
Title	Biological, clinical and population relevance of 95 loci for blood lipids.
Risk Allele	G
P-val	2E-9
Odds Ratio	0.9700 None

[PMID 21193429] Determinants of platelet count in humans.

Babies who are rs11065987(G;G) are about 1.3 times more likely to be born with tetralogy of Fallot (TOF) http://blog.23andme.com/23andme-research/snpwatch/snpwatch-common-genetic-factors-associated-with-blue-babies/

GWAS snp
PMID	[PMID 23297363]
Trait	Tetralogy of Fallot
Title	Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot.
Risk Allele	G
P-val	8E-11
Odds Ratio	1.34 [1.208-1.496]

GWAS snp
PMID	[PMID 24262325]
Trait	Coronary artery disease or ischemic stroke
Title	Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
Risk Allele
P-val	4E-14
Odds Ratio	NR NR

GWAS snp
PMID	[PMID 24097068]
Trait	Cholesterol, total
Title	Discovery and refinement of loci associated with lipid levels.
Risk Allele	G
P-val	2E-16
Odds Ratio	.03 [NR] unit decrease