rs17826255

Orientation

plus

Stabilized

plus

Make rs17826255(C;C)

Make rs17826255(C;T)

Make rs17826255(T;T)

Reference

GRCh38 38.1/141

Chromosome

17

Position

31006498

Gene	LOC107984974

is a	snp
is	mentioned by
dbSNP	rs17826255
dbSNP (classic)	rs17826255
ClinGen	rs17826255
ebi	rs17826255
HLI	rs17826255
Exac	rs17826255
Gnomad	rs17826255
Varsome	rs17826255
LitVar	rs17826255
Map	rs17826255
PheGenI	rs17826255
Biobank	rs17826255
1000 genomes	rs17826255
hgdp	rs17826255
ensembl	rs17826255
geneview	rs17826255
scholar	rs17826255
google	rs17826255
pharmgkb	rs17826255
gwascentral	rs17826255
openSNP	rs17826255
23andMe	rs17826255
SNPshot	rs17826255
SNPdbe	rs17826255
MSV3d	rs17826255
GWAS Ctlg	rs17826255

GMAF

0.07208

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23049088]
Trait	Myopia (pathological)
Title	A Genome-Wide Association Study Provides Evidence for Association of Chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with High Myopia in the French Population.
Risk Allele
P-val	8E-9
Odds Ratio	NR NR