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

rs4149311

From SNPedia

Orientationminus
Stabilizedminus
Make rs4149311(A;A)
Make rs4149311(A;G)
Make rs4149311(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position104826496
GeneABCA1
is asnp
is mentioned by
dbSNPrs4149311
ebirs4149311
HLIrs4149311
Exacrs4149311
Varsomers4149311
Maprs4149311
PheGenIrs4149311
hapmaprs4149311
1000 genomesrs4149311
hgdprs4149311
ensemblrs4149311
gopubmedrs4149311
geneviewrs4149311
scholarrs4149311
googlers4149311
pharmgkbrs4149311
gwascentralrs4149311
openSNPrs4149311
23andMers4149311
23andMe allrs4149311
SNP Nexus

SNPshotrs4149311
SNPdbers4149311
MSV3drs4149311
GWAS Ctlgrs4149311
GMAF0.3512
Max Magnitude
? (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 9E-6
Odds Ratio NR NR