rs772486760
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs772486760(-;TTTC) |
Make rs772486760(TTTC;TTTC) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 2 |
Position | 214781413 |
Gene | BARD1 |
is a | snp |
is | mentioned by |
dbSNP | rs772486760 |
dbSNP (classic) | rs772486760 |
ClinGen | rs772486760 |
ebi | rs772486760 |
HLI | rs772486760 |
Exac | rs772486760 |
Gnomad | rs772486760 |
Varsome | rs772486760 |
LitVar | rs772486760 |
Map | rs772486760 |
PheGenI | rs772486760 |
Biobank | rs772486760 |
1000 genomes | rs772486760 |
hgdp | rs772486760 |
ensembl | rs772486760 |
geneview | rs772486760 |
scholar | rs772486760 |
rs772486760 | |
pharmgkb | rs772486760 |
gwascentral | rs772486760 |
openSNP | rs772486760 |
23andMe | rs772486760 |
SNPshot | rs772486760 |
SNPdbe | rs772486760 |
MSV3d | rs772486760 |
GWAS Ctlg | rs772486760 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs772486760(CTTT;CTTT) |
Alt | rs772486760(CTTT;CTTT) |
Reference | Rs772486760(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | BARD1 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.215646138_215646141dupCTTT |
CLNSRC | |
CLNACC | RCV000220804.1, |