rs2071426

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs2071426(A;G)

Make rs2071426(G;G)

Reference

GRCh38 38.1/142

Chromosome

10

Position

95068566

Gene

CYP2C8

is a	snp
is	mentioned by
dbSNP	rs2071426
dbSNP (classic)	rs2071426
ClinGen	rs2071426
ebi	rs2071426
HLI	rs2071426
Exac	rs2071426
Gnomad	rs2071426
Varsome	rs2071426
LitVar	rs2071426
Map	rs2071426
PheGenI	rs2071426
Biobank	rs2071426
1000 genomes	rs2071426
hgdp	rs2071426
ensembl	rs2071426
geneview	rs2071426
scholar	rs2071426
google	rs2071426
pharmgkb	rs2071426
gwascentral	rs2071426
openSNP	rs2071426
23andMe	rs2071426
SNPshot	rs2071426
SNPdbe	rs2071426
MSV3d	rs2071426
GWAS Ctlg	rs2071426

Max Magnitude

0

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

GWAS snp
PMID	[PMID 24816252]
Trait	Blood metabolite levels
Title	An atlas of genetic influences on human blood metabolites.
Risk Allele	T
P-val	4E-14
Odds Ratio	.05 [0.038-0.066] unit increase

ClinVar
Risk	rs2071426(G;G)
Alt	rs2071426(G;G)
Reference	Rs2071426(A;A)
Significance	Non-pathogenic
Disease	not specified
Variation	info
Gene	CYP2C8
CLNDBN	not specified
Reversed	1
HGVS	NC_000010.10:g.96828323T>C
CLNSRC
CLNACC	RCV000454447.1,