rs11274804
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11274804(-;-) |
Make rs11274804(-;TCATTCCCTCTCCA) |
Make rs11274804(TCATTCCCTCTCCA;TCATTCCCTCTCCA) |
Reference | GRCh38 38.1/141 |
Chromosome | 2 |
Position | 40255057 |
Gene | SLC8A1, SLC8A1-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs11274804 |
dbSNP (classic) | rs11274804 |
ClinGen | rs11274804 |
ebi | rs11274804 |
HLI | rs11274804 |
Exac | rs11274804 |
Gnomad | rs11274804 |
Varsome | rs11274804 |
LitVar | rs11274804 |
Map | rs11274804 |
PheGenI | rs11274804 |
Biobank | rs11274804 |
1000 genomes | rs11274804 |
hgdp | rs11274804 |
ensembl | rs11274804 |
geneview | rs11274804 |
scholar | rs11274804 |
rs11274804 | |
pharmgkb | rs11274804 |
gwascentral | rs11274804 |
openSNP | rs11274804 |
23andMe | rs11274804 |
SNPshot | rs11274804 |
SNPdbe | rs11274804 |
MSV3d | rs11274804 |
GWAS Ctlg | rs11274804 |
Max Magnitude | 0 |
[PMID 20109173] Hypervariable intronic region in NCX1 is enriched in short insertion-deletion polymorphisms and showed association with cardiovascular traits