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rs6968355

From SNPedia

Orientationplus
Stabilizedplus
Make rs6968355(C;C)
Make rs6968355(C;T)
Make rs6968355(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position105117803
GeneSRPK2
is asnp
is mentioned by
dbSNPrs6968355
ebirs6968355
HLIrs6968355
Exacrs6968355
Varsomers6968355
Maprs6968355
PheGenIrs6968355
hapmaprs6968355
1000 genomesrs6968355
hgdprs6968355
ensemblrs6968355
gopubmedrs6968355
geneviewrs6968355
scholarrs6968355
googlers6968355
pharmgkbrs6968355
gwascentralrs6968355
openSNPrs6968355
23andMers6968355
23andMe allrs6968355
SNP Nexus

SNPshotrs6968355
SNPdbers6968355
MSV3drs6968355
GWAS Ctlgrs6968355
GMAF0.09458
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 2E-7
Odds Ratio NR NR