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rs9984974

From SNPedia

Orientationplus
Stabilizedplus
Make rs9984974(A;A)
Make rs9984974(A;G)
Make rs9984974(G;G)
ReferenceGRCh38 38.1/141
Chromosome21
Position36437079
is asnp
is mentioned by
dbSNPrs9984974
ebirs9984974
HLIrs9984974
Exacrs9984974
Varsomers9984974
Maprs9984974
PheGenIrs9984974
hapmaprs9984974
1000 genomesrs9984974
hgdprs9984974
ensemblrs9984974
gopubmedrs9984974
geneviewrs9984974
scholarrs9984974
googlers9984974
pharmgkbrs9984974
gwascentralrs9984974
openSNPrs9984974
23andMers9984974
23andMe allrs9984974
SNP Nexus

SNPshotrs9984974
SNPdbers9984974
MSV3drs9984974
GWAS Ctlgrs9984974
GMAF0.3205
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 2E-6
Odds Ratio NR NR