rs10488699
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs10488699(A;A) |
Make rs10488699(A;G) |
Make rs10488699(G;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 11 |
Position | 116761784 |
Gene | BUD13 |
is a | snp |
is | mentioned by |
dbSNP | rs10488699 |
dbSNP (classic) | rs10488699 |
ClinGen | rs10488699 |
ebi | rs10488699 |
HLI | rs10488699 |
Exac | rs10488699 |
Gnomad | rs10488699 |
Varsome | rs10488699 |
LitVar | rs10488699 |
Map | rs10488699 |
PheGenI | rs10488699 |
Biobank | rs10488699 |
1000 genomes | rs10488699 |
hgdp | rs10488699 |
ensembl | rs10488699 |
geneview | rs10488699 |
scholar | rs10488699 |
rs10488699 | |
pharmgkb | rs10488699 |
gwascentral | rs10488699 |
openSNP | rs10488699 |
23andMe | rs10488699 |
SNPshot | rs10488699 |
SNPdbe | rs10488699 |
MSV3d | rs10488699 |
GWAS Ctlg | rs10488699 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 28257648] Genetic determinants of clinical heterogeneity of the coronary artery disease in the population of Hyderabad, India.
[PMID 28610615] Quantitative trait loci at the 11q23.3 chromosomal region related to dyslipidemia in the population of Andhra Pradesh, India.