rs878853995
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs878853995(C;G) |
Make rs878853995(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 214780702 |
Gene | BARD1 |
is a | snp |
is | mentioned by |
dbSNP | rs878853995 |
dbSNP (classic) | rs878853995 |
ClinGen | rs878853995 |
ebi | rs878853995 |
HLI | rs878853995 |
Exac | rs878853995 |
Gnomad | rs878853995 |
Varsome | rs878853995 |
LitVar | rs878853995 |
Map | rs878853995 |
PheGenI | rs878853995 |
Biobank | rs878853995 |
1000 genomes | rs878853995 |
hgdp | rs878853995 |
ensembl | rs878853995 |
geneview | rs878853995 |
scholar | rs878853995 |
rs878853995 | |
pharmgkb | rs878853995 |
gwascentral | rs878853995 |
openSNP | rs878853995 |
23andMe | rs878853995 |
SNPshot | rs878853995 |
SNPdbe | rs878853995 |
MSV3d | rs878853995 |
GWAS Ctlg | rs878853995 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878853995(G;G) |
Alt | rs878853995(G;G) |
Reference | Rs878853995(C;C) |
Significance | Pathogenic |
Disease | Familial cancer of breast |
Variation | info |
Gene | BARD1 |
CLNDBN | Familial cancer of breast |
Reversed | 1 |
HGVS | NC_000002.11:g.215645426G>C |
CLNSRC | |
CLNACC | RCV000231412.1, |