rs876660623
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs876660623(-;-) |
Make rs876660623(-;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 43094279 |
Gene | BRCA1 |
is a | snp |
is | mentioned by |
dbSNP | rs876660623 |
dbSNP (classic) | rs876660623 |
ClinGen | rs876660623 |
ebi | rs876660623 |
HLI | rs876660623 |
Exac | rs876660623 |
Gnomad | rs876660623 |
Varsome | rs876660623 |
LitVar | rs876660623 |
Map | rs876660623 |
PheGenI | rs876660623 |
Biobank | rs876660623 |
1000 genomes | rs876660623 |
hgdp | rs876660623 |
ensembl | rs876660623 |
geneview | rs876660623 |
scholar | rs876660623 |
rs876660623 | |
pharmgkb | rs876660623 |
gwascentral | rs876660623 |
openSNP | rs876660623 |
23andMe | rs876660623 |
SNPshot | rs876660623 |
SNPdbe | rs876660623 |
MSV3d | rs876660623 |
GWAS Ctlg | rs876660623 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876660623(-;-) |
Alt | rs876660623(-;-) |
Reference | Rs876660623(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not provided |
Variation | info |
Gene | BRCA1 |
CLNDBN | Hereditary cancer-predisposing syndrome not provided |
Reversed | 1 |
HGVS | NC_000017.10:g.41246296delC |
CLNSRC | |
CLNACC | RCV000218101.1, RCV000484830.1, |