rs12205363

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0

Make rs12205363(C;C)

Make rs12205363(C;T)

Reference

GRCh38 38.1/141

Chromosome

6

Position

129513484

Gene	LAMA2, LOC102723409

is a	snp
is	mentioned by
dbSNP	rs12205363
dbSNP (classic)	rs12205363
ClinGen	rs12205363
ebi	rs12205363
HLI	rs12205363
Exac	rs12205363
Gnomad	rs12205363
Varsome	rs12205363
LitVar	rs12205363
Map	rs12205363
PheGenI	rs12205363
Biobank	rs12205363
1000 genomes	rs12205363
hgdp	rs12205363
ensembl	rs12205363
geneview	rs12205363
scholar	rs12205363
google	rs12205363
pharmgkb	rs12205363
gwascentral	rs12205363
openSNP	rs12205363
23andMe	rs12205363
SNPshot	rs12205363
SNPdbe	rs12205363
MSV3d	rs12205363
GWAS Ctlg	rs12205363

GMAF

0.03673

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23396134]
Trait	Refractive error
Title	Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia.
Risk Allele	C
P-val	2E-12
Odds Ratio	.24 [0.17-0.3] unit increase

Occurs within the LAMA2 (Laminin alpha-2) gene