rs879255318
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs879255318(-;TGGAATC) |
Make rs879255318(TGGAATC;TGGAATC) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 43071209 |
Gene | BRCA1 |
is a | snp |
is | mentioned by |
dbSNP | rs879255318 |
dbSNP (classic) | rs879255318 |
ClinGen | rs879255318 |
ebi | rs879255318 |
HLI | rs879255318 |
Exac | rs879255318 |
Gnomad | rs879255318 |
Varsome | rs879255318 |
LitVar | rs879255318 |
Map | rs879255318 |
PheGenI | rs879255318 |
Biobank | rs879255318 |
1000 genomes | rs879255318 |
hgdp | rs879255318 |
ensembl | rs879255318 |
geneview | rs879255318 |
scholar | rs879255318 |
rs879255318 | |
pharmgkb | rs879255318 |
gwascentral | rs879255318 |
openSNP | rs879255318 |
23andMe | rs879255318 |
SNPshot | rs879255318 |
SNPdbe | rs879255318 |
MSV3d | rs879255318 |
GWAS Ctlg | rs879255318 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879255318(TGGAATC;TGGAATC) |
Alt | rs879255318(TGGAATC;TGGAATC) |
Reference | Rs879255318(-;-) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | BRCA1 |
CLNDBN | not specified |
Reversed | 1 |
HGVS | NC_000017.10:g.41223227_41223233dupGATTCCA |
CLNSRC | |
CLNACC | RCV000238727.1, |