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rs55864141

From SNPedia

Orientationplus
Stabilizedplus
Make rs55864141(C;C)
Make rs55864141(C;T)
Make rs55864141(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position9949512
is asnp
is mentioned by
dbSNPrs55864141
ebirs55864141
HLIrs55864141
Exacrs55864141
Varsomers55864141
Maprs55864141
PheGenIrs55864141
hapmaprs55864141
1000 genomesrs55864141
hgdprs55864141
ensemblrs55864141
gopubmedrs55864141
geneviewrs55864141
scholarrs55864141
googlers55864141
pharmgkbrs55864141
gwascentralrs55864141
openSNPrs55864141
23andMers55864141
23andMe allrs55864141
SNP Nexus

SNPshotrs55864141
SNPdbers55864141
MSV3drs55864141
GWAS Ctlgrs55864141
GMAF0.3292
Max Magnitude

[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