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rs17822114

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0
Make rs17822114(C;T)
Make rs17822114(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position60699699
is asnp
is mentioned by
dbSNPrs17822114
ebirs17822114
HLIrs17822114
Exacrs17822114
Varsomers17822114
Maprs17822114
PheGenIrs17822114
hapmaprs17822114
1000 genomesrs17822114
hgdprs17822114
ensemblrs17822114
gopubmedrs17822114
geneviewrs17822114
scholarrs17822114
googlers17822114
pharmgkbrs17822114
gwascentralrs17822114
openSNPrs17822114
23andMers17822114
23andMe allrs17822114
SNP Nexus

SNPshotrs17822114
SNPdbers17822114
MSV3drs17822114
GWAS Ctlgrs17822114
GMAF0.04454
Max Magnitude0
? (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-18
Odds Ratio NR NR