rs1057519365
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(AA;AA) | 0 | common in clinvar |
Make rs1057519365(-;-) |
Make rs1057519365(-;AA) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 17 |
Position | 61780931 |
Gene | BRIP1 |
is a | snp |
is | mentioned by |
dbSNP | rs1057519365 |
dbSNP (classic) | rs1057519365 |
ClinGen | rs1057519365 |
ebi | rs1057519365 |
HLI | rs1057519365 |
Exac | rs1057519365 |
Gnomad | rs1057519365 |
Varsome | rs1057519365 |
LitVar | rs1057519365 |
Map | rs1057519365 |
PheGenI | rs1057519365 |
Biobank | rs1057519365 |
1000 genomes | rs1057519365 |
hgdp | rs1057519365 |
ensembl | rs1057519365 |
geneview | rs1057519365 |
scholar | rs1057519365 |
rs1057519365 | |
pharmgkb | rs1057519365 |
gwascentral | rs1057519365 |
openSNP | rs1057519365 |
23andMe | rs1057519365 |
SNPshot | rs1057519365 |
SNPdbe | rs1057519365 |
MSV3d | rs1057519365 |
GWAS Ctlg | rs1057519365 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057519365(-;-) |
Alt | rs1057519365(-;-) |
Reference | Rs1057519365(AA;AA) |
Significance | Probable-Pathogenic |
Disease | Carcinoma of colon not provided |
Variation | info |
Gene | BRIP1 |
CLNDBN | Carcinoma of colon not provided |
Reversed | 1 |
HGVS | NC_000017.10:g.59858292_59858293delTT |
CLNSRC | |
CLNACC | RCV000416663.1, RCV000477976.1, |