rs714
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs714(A;A) |
Make rs714(A;G) |
Make rs714(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 52992904 |
Gene | DCC |
is a | snp |
is | mentioned by |
dbSNP | rs714 |
dbSNP (classic) | rs714 |
ClinGen | rs714 |
ebi | rs714 |
HLI | rs714 |
Exac | rs714 |
Gnomad | rs714 |
Varsome | rs714 |
LitVar | rs714 |
Map | rs714 |
PheGenI | rs714 |
Biobank | rs714 |
1000 genomes | rs714 |
hgdp | rs714 |
ensembl | rs714 |
geneview | rs714 |
scholar | rs714 |
rs714 | |
pharmgkb | rs714 |
gwascentral | rs714 |
openSNP | rs714 |
23andMe | rs714 |
SNPshot | rs714 |
SNPdbe | rs714 |
MSV3d | rs714 |
GWAS Ctlg | rs714 |
GMAF | 0.2498 |
Max Magnitude | 0 |
[PMID 23353777] DCC (Deleted in Colorectal Carcinoma) Gene Variants Confer Increased Susceptibility to Gallbladder Cancer (Ref. No.: GENE-D-12-01446) [PMID 23765761] Role of genetic variants of deleted in colorectal carcinoma (DCC) polymorphisms and esophageal and gastric cancers risk in Kashmir Valley and meta-analysis. [PMID 26891331] Impact of DCC (rs714) and PSCA (rs2294008 and rs2976392) Gene Polymorphism in Modulating Cancer Risk in Asian Population.