rs55864141
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs55864141(C;C) |
Make rs55864141(C;T) |
Make rs55864141(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 9949512 |
is a | snp |
is | mentioned by |
dbSNP | rs55864141 |
dbSNP (classic) | rs55864141 |
ClinGen | rs55864141 |
ebi | rs55864141 |
HLI | rs55864141 |
Exac | rs55864141 |
Gnomad | rs55864141 |
Varsome | rs55864141 |
LitVar | rs55864141 |
Map | rs55864141 |
PheGenI | rs55864141 |
Biobank | rs55864141 |
1000 genomes | rs55864141 |
hgdp | rs55864141 |
ensembl | rs55864141 |
geneview | rs55864141 |
scholar | rs55864141 |
rs55864141 | |
pharmgkb | rs55864141 |
gwascentral | rs55864141 |
openSNP | rs55864141 |
23andMe | rs55864141 |
SNPshot | rs55864141 |
SNPdbe | rs55864141 |
MSV3d | rs55864141 |
GWAS Ctlg | rs55864141 |
GMAF | 0.3292 |
Max Magnitude | 0 |
[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