Have questions? Visit https://www.reddit.com/r/SNPedia

rs665440

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 normal
Make rs665440(A;G)
Make rs665440(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position128712662
GeneFLI1
is asnp
is mentioned by
dbSNPrs665440
dbSNP (classic)rs665440
ClinGenrs665440
ebirs665440
HLIrs665440
Exacrs665440
Gnomadrs665440
Varsomers665440
LitVarrs665440
Maprs665440
PheGenIrs665440
Biobankrs665440
1000 genomesrs665440
hgdprs665440
ensemblrs665440
geneviewrs665440
scholarrs665440
googlers665440
pharmgkbrs665440
gwascentralrs665440
openSNPrs665440
23andMers665440
SNPshotrs665440
SNPdbers665440
MSV3drs665440
GWAS Ctlgrs665440
GMAF0.05005
Max Magnitude0
? (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 2E-8
Odds Ratio NR NR