Have questions? Visit https://www.reddit.com/r/SNPedia

rs17103138

From SNPedia

Orientationplus
Stabilizedplus
Make rs17103138(C;C)
Make rs17103138(C;T)
Make rs17103138(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position122153815
GeneTACC2
is asnp
is mentioned by
dbSNPrs17103138
ebirs17103138
HLIrs17103138
Exacrs17103138
Varsomers17103138
Maprs17103138
PheGenIrs17103138
hapmaprs17103138
1000 genomesrs17103138
hgdprs17103138
ensemblrs17103138
gopubmedrs17103138
geneviewrs17103138
scholarrs17103138
googlers17103138
pharmgkbrs17103138
gwascentralrs17103138
openSNPrs17103138
23andMers17103138
23andMe allrs17103138
SNP Nexus

SNPshotrs17103138
SNPdbers17103138
MSV3drs17103138
GWAS Ctlgrs17103138
GMAF0.1157
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