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rs17155227

From SNPedia

Orientationplus
Stabilizedplus
Make rs17155227(C;C)
Make rs17155227(C;T)
Make rs17155227(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position9104480
is asnp
is mentioned by
dbSNPrs17155227
ebirs17155227
HLIrs17155227
Exacrs17155227
Varsomers17155227
Maprs17155227
PheGenIrs17155227
hapmaprs17155227
1000 genomesrs17155227
hgdprs17155227
ensemblrs17155227
gopubmedrs17155227
geneviewrs17155227
scholarrs17155227
googlers17155227
pharmgkbrs17155227
gwascentralrs17155227
openSNPrs17155227
23andMers17155227
23andMe allrs17155227
SNP Nexus

SNPshotrs17155227
SNPdbers17155227
MSV3drs17155227
GWAS Ctlgrs17155227
GMAF0.09458
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 23049088] A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French population