rs587781526
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(TCTATGATCTCTTTAGGGGT;TCTATGATCTCTTTAGGGGT) | 0 | common in clinvar |
Make rs587781526(AATA;AATA) |
Make rs587781526(AATA;TCTATGATCTCTTTAGGGGT) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 43063370 |
Gene | BRCA1 |
is a | snp |
is | mentioned by |
dbSNP | rs587781526 |
dbSNP (classic) | rs587781526 |
ClinGen | rs587781526 |
ebi | rs587781526 |
HLI | rs587781526 |
Exac | rs587781526 |
Gnomad | rs587781526 |
Varsome | rs587781526 |
LitVar | rs587781526 |
Map | rs587781526 |
PheGenI | rs587781526 |
Biobank | rs587781526 |
1000 genomes | rs587781526 |
hgdp | rs587781526 |
ensembl | rs587781526 |
geneview | rs587781526 |
scholar | rs587781526 |
rs587781526 | |
pharmgkb | rs587781526 |
gwascentral | rs587781526 |
openSNP | rs587781526 |
23andMe | rs587781526 |
SNPshot | rs587781526 |
SNPdbe | rs587781526 |
MSV3d | rs587781526 |
GWAS Ctlg | rs587781526 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587781526(AATA;AATA) |
Alt | rs587781526(AATA;AATA) |
Reference | Rs587781526(TCTATGATCTCTTTAGGGGT;TCTATGATCTCTTTAGGGGT) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | BRCA1 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000017.10:g.41215387_41215406del20insTATT |
CLNSRC | |
CLNACC | RCV000129518.1, |