rs656319

Orientation

minus

Stabilized

minus

Make rs656319(C;C)

Make rs656319(C;T)

Make rs656319(T;T)

Reference

GRCh38 38.1/142

Chromosome

8

Position

9956901

is a	snp
is	mentioned by
dbSNP	rs656319
dbSNP (classic)	rs656319
ClinGen	rs656319
ebi	rs656319
HLI	rs656319
Exac	rs656319
Gnomad	rs656319
Varsome	rs656319
LitVar	rs656319
Map	rs656319
PheGenI	rs656319
Biobank	rs656319
1000 genomes	rs656319
hgdp	rs656319
ensembl	rs656319
geneview	rs656319
scholar	rs656319
google	rs656319
pharmgkb	rs656319
gwascentral	rs656319
openSNP	rs656319
23andMe	rs656319
SNPshot	rs656319
SNPdbe	rs656319
MSV3d	rs656319
GWAS Ctlg	rs656319

GMAF

0.4128

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	3E-6
Odds Ratio	NR NR