rs875989791
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs875989791(-;A) |
Make rs875989791(A;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 16 |
Position | 23635852 |
Gene | PALB2 |
is a | snp |
is | mentioned by |
dbSNP | rs875989791 |
dbSNP (classic) | rs875989791 |
ClinGen | rs875989791 |
ebi | rs875989791 |
HLI | rs875989791 |
Exac | rs875989791 |
Gnomad | rs875989791 |
Varsome | rs875989791 |
LitVar | rs875989791 |
Map | rs875989791 |
PheGenI | rs875989791 |
Biobank | rs875989791 |
1000 genomes | rs875989791 |
hgdp | rs875989791 |
ensembl | rs875989791 |
geneview | rs875989791 |
scholar | rs875989791 |
rs875989791 | |
pharmgkb | rs875989791 |
gwascentral | rs875989791 |
openSNP | rs875989791 |
23andMe | rs875989791 |
SNPshot | rs875989791 |
SNPdbe | rs875989791 |
MSV3d | rs875989791 |
GWAS Ctlg | rs875989791 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs875989791(A;A) |
Alt | rs875989791(A;A) |
Reference | Rs875989791(-;-) |
Significance | Probable-Pathogenic |
Disease | Familial cancer of breast |
Variation | info |
Gene | PALB2 |
CLNDBN | Familial cancer of breast |
Reversed | 1 |
HGVS | NC_000016.9:g.23647174dupT |
CLNSRC | |
CLNACC | RCV000211082.1, |