rs3786800

Orientation

minus

Stabilized

minus

Make rs3786800(A;A)

Make rs3786800(A;G)

Make rs3786800(G;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

30499793

Gene

ZNF536

is a	snp
is	mentioned by
dbSNP	rs3786800
dbSNP (classic)	rs3786800
ClinGen	rs3786800
ebi	rs3786800
HLI	rs3786800
Exac	rs3786800
Gnomad	rs3786800
Varsome	rs3786800
LitVar	rs3786800
Map	rs3786800
PheGenI	rs3786800
Biobank	rs3786800
1000 genomes	rs3786800
hgdp	rs3786800
ensembl	rs3786800
geneview	rs3786800
scholar	rs3786800
google	rs3786800
pharmgkb	rs3786800
gwascentral	rs3786800
openSNP	rs3786800
23andMe	rs3786800
SNPshot	rs3786800
SNPdbe	rs3786800
MSV3d	rs3786800
GWAS Ctlg	rs3786800

GMAF

0.1791

Max Magnitude

0

?	(A;A) (A;G) (G;G)	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-12
Odds Ratio	NR NR