rs16943176
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs16943176(A;A) |
Make rs16943176(A;G) |
Make rs16943176(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 58692526 |
Gene | RAD51C, TEX14 |
is a | snp |
is | mentioned by |
dbSNP | rs16943176 |
dbSNP (classic) | rs16943176 |
ClinGen | rs16943176 |
ebi | rs16943176 |
HLI | rs16943176 |
Exac | rs16943176 |
Gnomad | rs16943176 |
Varsome | rs16943176 |
LitVar | rs16943176 |
Map | rs16943176 |
PheGenI | rs16943176 |
Biobank | rs16943176 |
1000 genomes | rs16943176 |
hgdp | rs16943176 |
ensembl | rs16943176 |
geneview | rs16943176 |
scholar | rs16943176 |
rs16943176 | |
pharmgkb | rs16943176 |
gwascentral | rs16943176 |
openSNP | rs16943176 |
23andMe | rs16943176 |
SNPshot | rs16943176 |
SNPdbe | rs16943176 |
MSV3d | rs16943176 |
GWAS Ctlg | rs16943176 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 24631219] Rad51C: a novel suppressor gene modulates the risk of head and neck cancer
[PMID 25343521] Single nucleotide polymorphisms in noncoding regions of Rad51C do not change the risk of unselected breast cancer but they modulate the level of oxidative stress and the DNA damage characteristics: a case-control study
[PMID 26406419] RAD51C mutation screening in high-risk patients from Serbian hereditary breast/ovarian cancer families