rs878855099
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(G;T) | 5 | PALB2-related cancer risk |
Make rs878855099(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 16 |
Position | 23635177 |
Gene | PALB2 |
is a | snp |
is | mentioned by |
dbSNP | rs878855099 |
dbSNP (classic) | rs878855099 |
ClinGen | rs878855099 |
ebi | rs878855099 |
HLI | rs878855099 |
Exac | rs878855099 |
Gnomad | rs878855099 |
Varsome | rs878855099 |
LitVar | rs878855099 |
Map | rs878855099 |
PheGenI | rs878855099 |
Biobank | rs878855099 |
1000 genomes | rs878855099 |
hgdp | rs878855099 |
ensembl | rs878855099 |
geneview | rs878855099 |
scholar | rs878855099 |
rs878855099 | |
pharmgkb | rs878855099 |
gwascentral | rs878855099 |
openSNP | rs878855099 |
23andMe | rs878855099 |
SNPshot | rs878855099 |
SNPdbe | rs878855099 |
MSV3d | rs878855099 |
GWAS Ctlg | rs878855099 |
Max Magnitude | 5 |
ClinVar | |
---|---|
Risk | rs878855099(T;T) |
Alt | rs878855099(T;T) |
Reference | Rs878855099(G;G) |
Significance | Pathogenic |
Disease | Familial cancer of breast |
Variation | info |
Gene | PALB2 |
CLNDBN | Familial cancer of breast |
Reversed | 1 |
HGVS | NC_000016.9:g.23646498C>A |
CLNSRC | |
CLNACC | RCV000231944.1, |