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rs7428796

From SNPedia

Orientationplus
Stabilizedplus
Make rs7428796(C;C)
Make rs7428796(C;T)
Make rs7428796(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position86206522
is asnp
is mentioned by
dbSNPrs7428796
ebirs7428796
HLIrs7428796
Exacrs7428796
Varsomers7428796
Maprs7428796
PheGenIrs7428796
hapmaprs7428796
1000 genomesrs7428796
hgdprs7428796
ensemblrs7428796
gopubmedrs7428796
geneviewrs7428796
scholarrs7428796
googlers7428796
pharmgkbrs7428796
gwascentralrs7428796
openSNPrs7428796
23andMers7428796
23andMe allrs7428796
SNP Nexus

SNPshotrs7428796
SNPdbers7428796
MSV3drs7428796
GWAS Ctlgrs7428796
GMAF0.4757
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-18
Odds Ratio NR NR