rs876658348
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs876658348(-;-) |
Make rs876658348(-;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 16 |
Position | 23629684 |
Gene | PALB2 |
is a | snp |
is | mentioned by |
dbSNP | rs876658348 |
dbSNP (classic) | rs876658348 |
ClinGen | rs876658348 |
ebi | rs876658348 |
HLI | rs876658348 |
Exac | rs876658348 |
Gnomad | rs876658348 |
Varsome | rs876658348 |
LitVar | rs876658348 |
Map | rs876658348 |
PheGenI | rs876658348 |
Biobank | rs876658348 |
1000 genomes | rs876658348 |
hgdp | rs876658348 |
ensembl | rs876658348 |
geneview | rs876658348 |
scholar | rs876658348 |
rs876658348 | |
pharmgkb | rs876658348 |
gwascentral | rs876658348 |
openSNP | rs876658348 |
23andMe | rs876658348 |
SNPshot | rs876658348 |
SNPdbe | rs876658348 |
MSV3d | rs876658348 |
GWAS Ctlg | rs876658348 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876658348(-;-) |
Alt | rs876658348(-;-) |
Reference | Rs876658348(T;T) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | PALB2 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000016.9:g.23641005delA |
CLNSRC | |
CLNACC | RCV000217072.2, |