rs17690232

Orientation

plus

Stabilized

plus

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

Make rs17690232(C;G)

Make rs17690232(G;G)

Reference

GRCh38 38.1/141

Chromosome

4

Position

54368658

is a	snp
is	mentioned by
dbSNP	rs17690232
dbSNP (classic)	rs17690232
ClinGen	rs17690232
ebi	rs17690232
HLI	rs17690232
Exac	rs17690232
Gnomad	rs17690232
Varsome	rs17690232
LitVar	rs17690232
Map	rs17690232
PheGenI	rs17690232
Biobank	rs17690232
1000 genomes	rs17690232
hgdp	rs17690232
ensembl	rs17690232
geneview	rs17690232
scholar	rs17690232
google	rs17690232
pharmgkb	rs17690232
gwascentral	rs17690232
openSNP	rs17690232
23andMe	rs17690232
SNPshot	rs17690232
SNPdbe	rs17690232
MSV3d	rs17690232
GWAS Ctlg	rs17690232

GMAF

0.09642

Max Magnitude

0

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

GWAS
SNP	rs17690232
PubMedID	[PMID 18193045]
Condition	Height
Gene	PDGFRA
Risk Allele	C
pValue	4.00E-007
OR	0.86
95% CI	NR) cm talle