rs10492681

Orientation

plus

Stabilized

plus

Make rs10492681(C;C)

Make rs10492681(C;G)

Make rs10492681(G;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

40233346

is a	snp
is	mentioned by
dbSNP	rs10492681
dbSNP (classic)	rs10492681
ClinGen	rs10492681
ebi	rs10492681
HLI	rs10492681
Exac	rs10492681
Gnomad	rs10492681
Varsome	rs10492681
LitVar	rs10492681
Map	rs10492681
PheGenI	rs10492681
Biobank	rs10492681
1000 genomes	rs10492681
hgdp	rs10492681
ensembl	rs10492681
geneview	rs10492681
scholar	rs10492681
google	rs10492681
pharmgkb	rs10492681
gwascentral	rs10492681
openSNP	rs10492681
23andMe	rs10492681
SNPshot	rs10492681
SNPdbe	rs10492681
MSV3d	rs10492681
GWAS Ctlg	rs10492681

GMAF

0.3062

Max Magnitude

0

?	(C;C) (C;G) (G;G)	28

GWAS snp
PMID	[PMID 17903293]
Trait	Select biomarker traits
Title	Genome-wide association with select biomarker traits in the Framingham Heart Study
Risk Allele
P-val	0.0000019999999999999999
Odds Ratio	NR NR