rs879255313
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AA;AA) | 0 | common in clinvar |
Make rs879255313(-;-) |
Make rs879255313(-;AA) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 43094388 |
Gene | BRCA1 |
is a | snp |
is | mentioned by |
dbSNP | rs879255313 |
dbSNP (classic) | rs879255313 |
ClinGen | rs879255313 |
ebi | rs879255313 |
HLI | rs879255313 |
Exac | rs879255313 |
Gnomad | rs879255313 |
Varsome | rs879255313 |
LitVar | rs879255313 |
Map | rs879255313 |
PheGenI | rs879255313 |
Biobank | rs879255313 |
1000 genomes | rs879255313 |
hgdp | rs879255313 |
ensembl | rs879255313 |
geneview | rs879255313 |
scholar | rs879255313 |
rs879255313 | |
pharmgkb | rs879255313 |
gwascentral | rs879255313 |
openSNP | rs879255313 |
23andMe | rs879255313 |
SNPshot | rs879255313 |
SNPdbe | rs879255313 |
MSV3d | rs879255313 |
GWAS Ctlg | rs879255313 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879255313(-;-) |
Alt | rs879255313(-;-) |
Reference | Rs879255313(AA;AA) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | BRCA1 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000017.10:g.41246405_41246406delTT |
CLNSRC | |
CLNACC | RCV000239120.1, |