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rs656319

From SNPedia

Orientationminus
Stabilizedplus
Make rs656319(C;C)
Make rs656319(C;T)
Make rs656319(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position9956901
is asnp
is mentioned by
dbSNPrs656319
ebirs656319
HLIrs656319
Exacrs656319
Varsomers656319
Maprs656319
PheGenIrs656319
hapmaprs656319
1000 genomesrs656319
hgdprs656319
ensemblrs656319
gopubmedrs656319
geneviewrs656319
scholarrs656319
googlers656319
pharmgkbrs656319
gwascentralrs656319
openSNPrs656319
23andMers656319
23andMe allrs656319
SNP Nexus

SNPshotrs656319
SNPdbers656319
MSV3drs656319
GWAS Ctlgrs656319
GMAF0.4128
Max Magnitude
? (C;C) (C;T) (T;T) 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 3E-6
Odds Ratio NR NR