rs4860
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs4860(C;C) |
Make rs4860(C;T) |
Reference | GRCh37.p2 37.2/134 |
Chromosome | 12 |
Position | 63359783 |
Gene | RPL14 |
is a | snp |
is | mentioned by |
dbSNP | rs4860 |
dbSNP (classic) | rs4860 |
ClinGen | rs4860 |
ebi | rs4860 |
HLI | rs4860 |
Exac | rs4860 |
Gnomad | rs4860 |
Varsome | rs4860 |
LitVar | rs4860 |
Map | rs4860 |
PheGenI | rs4860 |
Biobank | rs4860 |
1000 genomes | rs4860 |
hgdp | rs4860 |
ensembl | rs4860 |
geneview | rs4860 |
scholar | rs4860 |
rs4860 | |
pharmgkb | rs4860 |
gwascentral | rs4860 |
openSNP | rs4860 |
23andMe | rs4860 |
SNPshot | rs4860 |
SNPdbe | rs4860 |
MSV3d | rs4860 |
GWAS Ctlg | rs4860 |
Max Magnitude | 0 |
[PMID 19551860] Common germline polymorphisms in COMT, CYP19A1, ESR1, PGR, SULT1E1 and STS and survival after a diagnosis of breast cancer [PMID 21080103] Catechol-O-methyltransferase (COMT) val158met polymorphism as a risk factor for PTSD after urban violence.
[PMID 26025199] Voxelwise eigenvector centrality mapping of the human functional connectome reveals an influence of the catechol-O-methyltransferase val158met polymorphism on the default mode and somatomotor network