rs10931753

Orientation

plus

Stabilized

plus

Make rs10931753(C;C)

Make rs10931753(C;G)

Make rs10931753(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

153712244

is a	snp
is	mentioned by
dbSNP	rs10931753
dbSNP (classic)	rs10931753
ClinGen	rs10931753
ebi	rs10931753
HLI	rs10931753
Exac	rs10931753
Gnomad	rs10931753
Varsome	rs10931753
LitVar	rs10931753
Map	rs10931753
PheGenI	rs10931753
Biobank	rs10931753
1000 genomes	rs10931753
hgdp	rs10931753
ensembl	rs10931753
geneview	rs10931753
scholar	rs10931753
google	rs10931753
pharmgkb	rs10931753
gwascentral	rs10931753
openSNP	rs10931753
23andMe	rs10931753
SNPshot	rs10931753
SNPdbe	rs10931753
MSV3d	rs10931753
GWAS Ctlg	rs10931753

GMAF

0.377

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23720494]
Trait	Blood trace element (Zn levels)
Title	Genome-wide association study identifies loci affecting blood copper, selenium and zinc.
Risk Allele
P-val	5E-6
Odds Ratio	.13 [0.074-0.184] unit increase