rs12946397
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs12946397(C;T) |
Make rs12946397(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 17 |
Position | 58692618 |
Gene | RAD51C, TEX14 |
is a | snp |
is | mentioned by |
dbSNP | rs12946397 |
dbSNP (classic) | rs12946397 |
ClinGen | rs12946397 |
ebi | rs12946397 |
HLI | rs12946397 |
Exac | rs12946397 |
Gnomad | rs12946397 |
Varsome | rs12946397 |
LitVar | rs12946397 |
Map | rs12946397 |
PheGenI | rs12946397 |
Biobank | rs12946397 |
1000 genomes | rs12946397 |
hgdp | rs12946397 |
ensembl | rs12946397 |
geneview | rs12946397 |
scholar | rs12946397 |
rs12946397 | |
pharmgkb | rs12946397 |
gwascentral | rs12946397 |
openSNP | rs12946397 |
23andMe | rs12946397 |
SNPshot | rs12946397 |
SNPdbe | rs12946397 |
MSV3d | rs12946397 |
GWAS Ctlg | rs12946397 |
Max Magnitude | 0 |
[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
ClinVar | |
---|---|
Risk | rs12946397(T;T) |
Alt | rs12946397(T;T) |
Reference | Rs12946397(C;C) |
Significance | Probable-non-pathogenic |
Disease | Breast and Ovarian Cancer Susceptibility Fanconi anemia |
Variation | info |
Gene | TEX14 RAD51C |
CLNDBN | Breast and Ovarian Cancer Susceptibility Fanconi anemia |
Reversed | 0 |
HGVS | NC_000017.10:g.56769979C>T |
CLNSRC | |
CLNACC | RCV000269140.1, RCV000381874.1, |