rs142697907
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs142697907(A;A) |
Make rs142697907(A;G) |
Make rs142697907(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 214510163 |
Gene | PTPN14 |
is a | snp |
is | mentioned by |
dbSNP | rs142697907 |
dbSNP (classic) | rs142697907 |
ClinGen | rs142697907 |
ebi | rs142697907 |
HLI | rs142697907 |
Exac | rs142697907 |
Gnomad | rs142697907 |
Varsome | rs142697907 |
LitVar | rs142697907 |
Map | rs142697907 |
PheGenI | rs142697907 |
Biobank | rs142697907 |
1000 genomes | rs142697907 |
hgdp | rs142697907 |
ensembl | rs142697907 |
geneview | rs142697907 |
scholar | rs142697907 |
rs142697907 | |
pharmgkb | rs142697907 |
gwascentral | rs142697907 |
openSNP | rs142697907 |
23andMe | rs142697907 |
SNPshot | rs142697907 |
SNPdbe | rs142697907 |
MSV3d | rs142697907 |
GWAS Ctlg | rs142697907 |
Max Magnitude | 0 |
[PMID 27485598] Genetic variations in the Hippo signaling pathway and breast cancer risk in African American women in the AMBER Consortium.