rs41273215
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs41273215(C;C) |
Make rs41273215(C;T) |
Make rs41273215(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 1 |
Position | 156912167 |
Gene | PEAR1 |
is a | snp |
is | mentioned by |
dbSNP | rs41273215 |
dbSNP (classic) | rs41273215 |
ClinGen | rs41273215 |
ebi | rs41273215 |
HLI | rs41273215 |
Exac | rs41273215 |
Gnomad | rs41273215 |
Varsome | rs41273215 |
LitVar | rs41273215 |
Map | rs41273215 |
PheGenI | rs41273215 |
Biobank | rs41273215 |
1000 genomes | rs41273215 |
hgdp | rs41273215 |
ensembl | rs41273215 |
geneview | rs41273215 |
scholar | rs41273215 |
rs41273215 | |
pharmgkb | rs41273215 |
gwascentral | rs41273215 |
openSNP | rs41273215 |
23andMe | rs41273215 |
SNPshot | rs41273215 |
SNPdbe | rs41273215 |
MSV3d | rs41273215 |
GWAS Ctlg | rs41273215 |
Max Magnitude | 0 |
[PMID 29867494] Variants of PEAR1 Are Associated With Outcome in Patients With ACS and Stable CAD Undergoing PCI.