rs6857559

Orientation

plus

Stabilized

plus

Make rs6857559(C;C)

Make rs6857559(C;T)

Make rs6857559(T;T)

Reference

GRCh38 38.1/141

Chromosome

4

Position

188199757

is a	snp
is	mentioned by
dbSNP	rs6857559
dbSNP (classic)	rs6857559
ClinGen	rs6857559
ebi	rs6857559
HLI	rs6857559
Exac	rs6857559
Gnomad	rs6857559
Varsome	rs6857559
LitVar	rs6857559
Map	rs6857559
PheGenI	rs6857559
Biobank	rs6857559
1000 genomes	rs6857559
hgdp	rs6857559
ensembl	rs6857559
geneview	rs6857559
scholar	rs6857559
google	rs6857559
pharmgkb	rs6857559
gwascentral	rs6857559
openSNP	rs6857559
23andMe	rs6857559
SNPshot	rs6857559
SNPdbe	rs6857559
MSV3d	rs6857559
GWAS Ctlg	rs6857559

GMAF

0.2842

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-21
Odds Ratio	NR NR