rs10495712
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10495712(A;A) |
Make rs10495712(A;G) |
Make rs10495712(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 20973240 |
is a | snp |
is | mentioned by |
dbSNP | rs10495712 |
dbSNP (classic) | rs10495712 |
ClinGen | rs10495712 |
ebi | rs10495712 |
HLI | rs10495712 |
Exac | rs10495712 |
Gnomad | rs10495712 |
Varsome | rs10495712 |
LitVar | rs10495712 |
Map | rs10495712 |
PheGenI | rs10495712 |
Biobank | rs10495712 |
1000 genomes | rs10495712 |
hgdp | rs10495712 |
ensembl | rs10495712 |
geneview | rs10495712 |
scholar | rs10495712 |
rs10495712 | |
pharmgkb | rs10495712 |
gwascentral | rs10495712 |
openSNP | rs10495712 |
23andMe | rs10495712 |
SNPshot | rs10495712 |
SNPdbe | rs10495712 |
MSV3d | rs10495712 |
GWAS Ctlg | rs10495712 |
GMAF | 0.1648 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 23262498] Impact of geneticfactorsondyslipidemia in HIV-infected patients starting antiretroviral therapy