rs13063604
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13063604(A;A) |
Make rs13063604(A;G) |
Make rs13063604(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 128085887 |
Gene | RUVBL1 |
is a | snp |
is | mentioned by |
dbSNP | rs13063604 |
dbSNP (classic) | rs13063604 |
ClinGen | rs13063604 |
ebi | rs13063604 |
HLI | rs13063604 |
Exac | rs13063604 |
Gnomad | rs13063604 |
Varsome | rs13063604 |
LitVar | rs13063604 |
Map | rs13063604 |
PheGenI | rs13063604 |
Biobank | rs13063604 |
1000 genomes | rs13063604 |
hgdp | rs13063604 |
ensembl | rs13063604 |
geneview | rs13063604 |
scholar | rs13063604 |
rs13063604 | |
pharmgkb | rs13063604 |
gwascentral | rs13063604 |
openSNP | rs13063604 |
23andMe | rs13063604 |
SNPshot | rs13063604 |
SNPdbe | rs13063604 |
MSV3d | rs13063604 |
GWAS Ctlg | rs13063604 |
GMAF | 0.185 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 20635389] Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancer [PMID 19543528] Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancer.