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rs7031748

From SNPedia

Merged intors2853579
Orientationminus
Stabilizedminus
Make rs7031748(A;A)
Make rs7031748(A;C)
Make rs7031748(C;C)
ReferenceGRCh38 38.1/141
Chromosome9
Position104828991
GeneABCA1
is asnp
is mentioned by
dbSNPrs7031748
ebirs7031748
HLIrs7031748
Exacrs7031748
Varsomers7031748
Maprs7031748
PheGenIrs7031748
hapmaprs7031748
1000 genomesrs7031748
hgdprs7031748
ensemblrs7031748
gopubmedrs7031748
geneviewrs7031748
scholarrs7031748
googlers7031748
pharmgkbrs7031748
gwascentralrs7031748
openSNPrs7031748
23andMers7031748
23andMe allrs7031748
SNP Nexus

SNPshotrs7031748
SNPdbers7031748
MSV3drs7031748
GWAS Ctlgrs7031748
StatusMerged into rs2853579
Max Magnitude
? (A;A) (A;C) (C;C) 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 8E-6
Odds Ratio NR NR