rs587776419
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 5 | PALB2-related cancer risk |
(C;G) | 5 | PALB2-related cancer risk |
(G;G) | 0 | common in clinvar |
(G;T) | 3 | significantly increased risk of breast cancer |
(T;T) | 7 | Fanconi anemia, complementation group N |
Reference | GRCh38 38.1/142 |
Chromosome | 16 |
Position | 23624008 |
Gene | PALB2 |
is a | snp |
is | mentioned by |
dbSNP | rs587776419 |
dbSNP (classic) | rs587776419 |
ClinGen | rs587776419 |
ebi | rs587776419 |
HLI | rs587776419 |
Exac | rs587776419 |
Gnomad | rs587776419 |
Varsome | rs587776419 |
LitVar | rs587776419 |
Map | rs587776419 |
PheGenI | rs587776419 |
Biobank | rs587776419 |
1000 genomes | rs587776419 |
hgdp | rs587776419 |
ensembl | rs587776419 |
geneview | rs587776419 |
scholar | rs587776419 |
rs587776419 | |
pharmgkb | rs587776419 |
gwascentral | rs587776419 |
openSNP | rs587776419 |
23andMe | rs587776419 |
SNPshot | rs587776419 |
SNPdbe | rs587776419 |
MSV3d | rs587776419 |
GWAS Ctlg | rs587776419 |
Max Magnitude | 7 |
ClinVar | |
---|---|
Risk | rs587776419(A;A) Rs587776419(T;T) |
Alt | rs587776419(A;A) Rs587776419(T;T) |
Reference | Rs587776419(G;G) |
Significance | Other |
Disease | not provided Familial cancer of breast |
Variation | info |
Gene | PALB2 |
CLNDBN | not provided Familial cancer of breast |
Reversed | 1 |
HGVS | NC_000016.9:g.23635329C>A; NC_000016.9:g.23635329C>T |
CLNSRC | ClinVar |
CLNACC | RCV000133481.2, RCV000411304.1, RCV000160847.1, |