rs1490388

Orientation

plus

Stabilized

plus

Make rs1490388(C;C)

Make rs1490388(C;T)

Make rs1490388(T;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

126514509

is a	snp
is	mentioned by
dbSNP	rs1490388
dbSNP (classic)	rs1490388
ClinGen	rs1490388
ebi	rs1490388
HLI	rs1490388
Exac	rs1490388
Gnomad	rs1490388
Varsome	rs1490388
LitVar	rs1490388
Map	rs1490388
PheGenI	rs1490388
Biobank	rs1490388
1000 genomes	rs1490388
hgdp	rs1490388
ensembl	rs1490388
geneview	rs1490388
scholar	rs1490388
google	rs1490388
pharmgkb	rs1490388
gwascentral	rs1490388
openSNP	rs1490388
23andMe	rs1490388
SNPshot	rs1490388
SNPdbe	rs1490388
MSV3d	rs1490388
GWAS Ctlg	rs1490388

GMAF

0.4389

Max Magnitude

0

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

GWAS snp
PMID	[PMID 18391951]
Trait	Height
Title	Many sequence variants affecting diversity of adult human height
Risk Allele	T
P-val	5.9999999999999997E-7
Odds Ratio	4.80 [2.84-6.76] % SD taller

[PMID 20546612] The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.