rs1049112
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1049112(A;A) |
Make rs1049112(A;G) |
Make rs1049112(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 10930757 |
Gene | PRH1, PRH1-PRR4, PRH2 |
is a | snp |
is | mentioned by |
dbSNP | rs1049112 |
dbSNP (classic) | rs1049112 |
ClinGen | rs1049112 |
ebi | rs1049112 |
HLI | rs1049112 |
Exac | rs1049112 |
Gnomad | rs1049112 |
Varsome | rs1049112 |
LitVar | rs1049112 |
Map | rs1049112 |
PheGenI | rs1049112 |
Biobank | rs1049112 |
1000 genomes | rs1049112 |
hgdp | rs1049112 |
ensembl | rs1049112 |
geneview | rs1049112 |
scholar | rs1049112 |
rs1049112 | |
pharmgkb | rs1049112 |
gwascentral | rs1049112 |
openSNP | rs1049112 |
23andMe | rs1049112 |
SNPshot | rs1049112 |
SNPdbe | rs1049112 |
MSV3d | rs1049112 |
GWAS Ctlg | rs1049112 |
Max Magnitude | 0 |
[PMID 28824325] Impacts of CCL4 gene polymorphisms on hepatocellular carcinoma susceptibility and development.