rs1057517539
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1057517539(A;A) |
Make rs1057517539(A;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 16 |
Position | 23629214 |
Gene | PALB2 |
is a | snp |
is | mentioned by |
dbSNP | rs1057517539 |
dbSNP (classic) | rs1057517539 |
ClinGen | rs1057517539 |
ebi | rs1057517539 |
HLI | rs1057517539 |
Exac | rs1057517539 |
Gnomad | rs1057517539 |
Varsome | rs1057517539 |
LitVar | rs1057517539 |
Map | rs1057517539 |
PheGenI | rs1057517539 |
Biobank | rs1057517539 |
1000 genomes | rs1057517539 |
hgdp | rs1057517539 |
ensembl | rs1057517539 |
geneview | rs1057517539 |
scholar | rs1057517539 |
rs1057517539 | |
pharmgkb | rs1057517539 |
gwascentral | rs1057517539 |
openSNP | rs1057517539 |
23andMe | rs1057517539 |
SNPshot | rs1057517539 |
SNPdbe | rs1057517539 |
MSV3d | rs1057517539 |
GWAS Ctlg | rs1057517539 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057517539(A;A) |
Alt | rs1057517539(A;A) |
Reference | Rs1057517539(C;C) |
Significance | Pathogenic |
Disease | Familial cancer of breast Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | PALB2 |
CLNDBN | Familial cancer of breast Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000016.9:g.23640535G>T |
CLNSRC | |
CLNACC | RCV000410429.1, RCV000454290.1, |