rs494562

Orientation

minus

Stabilized

minus

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

Make rs494562(C;C)

Make rs494562(C;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

85407411

is a	snp
is	mentioned by
dbSNP	rs494562
dbSNP (classic)	rs494562
ClinGen	rs494562
ebi	rs494562
HLI	rs494562
Exac	rs494562
Gnomad	rs494562
Varsome	rs494562
LitVar	rs494562
Map	rs494562
PheGenI	rs494562
Biobank	rs494562
1000 genomes	rs494562
hgdp	rs494562
ensembl	rs494562
geneview	rs494562
scholar	rs494562
google	rs494562
pharmgkb	rs494562
gwascentral	rs494562
openSNP	rs494562
23andMe	rs494562
SNPshot	rs494562
SNPdbe	rs494562
MSV3d	rs494562
GWAS Ctlg	rs494562

GMAF

0.1529

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 21886157]
Trait
Title	Human metabolic individuality in biomedical and pharmaceutical research.
Risk Allele	G
P-val	7E-13
Odds Ratio	0.3020 None

GWAS snp
PMID	[PMID 24816252]
Trait	Blood metabolite levels
Title	An atlas of genetic influences on human blood metabolites.
Risk Allele	A
P-val	1E-12
Odds Ratio	.12 [0.085-0.151] unit decrease