rs6734238

Orientation

plus

Stabilized

plus

Make rs6734238(A;A)

Make rs6734238(A;G)

Make rs6734238(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

113083453

is a	snp
is	mentioned by
dbSNP	rs6734238
dbSNP (classic)	rs6734238
ClinGen	rs6734238
ebi	rs6734238
HLI	rs6734238
Exac	rs6734238
Gnomad	rs6734238
Varsome	rs6734238
LitVar	rs6734238
Map	rs6734238
PheGenI	rs6734238
Biobank	rs6734238
1000 genomes	rs6734238
hgdp	rs6734238
ensembl	rs6734238
geneview	rs6734238
scholar	rs6734238
google	rs6734238
pharmgkb	rs6734238
gwascentral	rs6734238
openSNP	rs6734238
23andMe	rs6734238
SNPshot	rs6734238
SNPdbe	rs6734238
MSV3d	rs6734238
GWAS Ctlg	rs6734238

GMAF

0.3163

Max Magnitude

0

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

GWAS snp
PMID	[PMID 21300955]
Trait
Title	Meta-Analysis of Genome-Wide Association Studies in >80 000 Subjects Identifies Multiple Loci for C-Reactive Protein Levels
Risk Allele	G
P-val	2E-17
Odds Ratio	0.0500 [0.04-0.06] unit increase

GWAS snp
PMID	[PMID 22939635]
Trait	C-reactive protein
Title	Genome-wide association and population genetic analysis of C-reactive protein in African American and Hispanic American women.
Risk Allele	G
P-val	9E-10
Odds Ratio	.11 [0.073-0.143] unit decrease

GWAS snp
PMID	[PMID 23969696]
Trait	Fibrinogen
Title	Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease.
Risk Allele	A
P-val	6E-19
Odds Ratio	.01 [0.007-0.011] unit decrease

[PMID 30476131] Mendelian randomization analysis of C-reactive protein on colorectal cancer risk.