rs17038182

Orientation

plus

Stabilized

plus

Make rs17038182(C;C)

Make rs17038182(C;G)

Make rs17038182(G;G)

Reference

GRCh38 38.1/141

Chromosome

1

Position

118325782

is a	snp
is	mentioned by
dbSNP	rs17038182
dbSNP (classic)	rs17038182
ClinGen	rs17038182
ebi	rs17038182
HLI	rs17038182
Exac	rs17038182
Gnomad	rs17038182
Varsome	rs17038182
LitVar	rs17038182
Map	rs17038182
PheGenI	rs17038182
Biobank	rs17038182
1000 genomes	rs17038182
hgdp	rs17038182
ensembl	rs17038182
geneview	rs17038182
scholar	rs17038182
google	rs17038182
pharmgkb	rs17038182
gwascentral	rs17038182
openSNP	rs17038182
23andMe	rs17038182
SNPshot	rs17038182
SNPdbe	rs17038182
MSV3d	rs17038182
GWAS Ctlg	rs17038182

GMAF

0.2833

Max Magnitude

0

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

GWAS snp
PMID	[PMID 19396169]
Trait	Height
Title	A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits
Risk Allele	C
P-val	5E-7
Odds Ratio	0.30 [0.18-0.42] cm decrease

[PMID 20027299] Transferability and fine-mapping of genome-wide associated loci for adult height across human populations.