rs876658695
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs876658695(-;ATTG) |
Make rs876658695(ATTG;ATTG) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 16 |
Position | 23603543 |
Gene | PALB2 |
is a | snp |
is | mentioned by |
dbSNP | rs876658695 |
dbSNP (classic) | rs876658695 |
ClinGen | rs876658695 |
ebi | rs876658695 |
HLI | rs876658695 |
Exac | rs876658695 |
Gnomad | rs876658695 |
Varsome | rs876658695 |
LitVar | rs876658695 |
Map | rs876658695 |
PheGenI | rs876658695 |
Biobank | rs876658695 |
1000 genomes | rs876658695 |
hgdp | rs876658695 |
ensembl | rs876658695 |
geneview | rs876658695 |
scholar | rs876658695 |
rs876658695 | |
pharmgkb | rs876658695 |
gwascentral | rs876658695 |
openSNP | rs876658695 |
23andMe | rs876658695 |
SNPshot | rs876658695 |
SNPdbe | rs876658695 |
MSV3d | rs876658695 |
GWAS Ctlg | rs876658695 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876658695(ATTG;ATTG) |
Alt | rs876658695(ATTG;ATTG) |
Reference | Rs876658695(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | PALB2 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000016.9:g.23614865_23614868dupCAAT |
CLNSRC | |
CLNACC | RCV000219269.1, |