rs1060502684
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(TC;TC) | 0 | common in clinvar |
Make rs1060502684(-;-) |
Make rs1060502684(-;TC) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 22 |
Position | 28695829 |
Gene | CHEK2 |
is a | snp |
is | mentioned by |
dbSNP | rs1060502684 |
dbSNP (classic) | rs1060502684 |
ClinGen | rs1060502684 |
ebi | rs1060502684 |
HLI | rs1060502684 |
Exac | rs1060502684 |
Gnomad | rs1060502684 |
Varsome | rs1060502684 |
LitVar | rs1060502684 |
Map | rs1060502684 |
PheGenI | rs1060502684 |
Biobank | rs1060502684 |
1000 genomes | rs1060502684 |
hgdp | rs1060502684 |
ensembl | rs1060502684 |
geneview | rs1060502684 |
scholar | rs1060502684 |
rs1060502684 | |
pharmgkb | rs1060502684 |
gwascentral | rs1060502684 |
openSNP | rs1060502684 |
23andMe | rs1060502684 |
SNPshot | rs1060502684 |
SNPdbe | rs1060502684 |
MSV3d | rs1060502684 |
GWAS Ctlg | rs1060502684 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1060502684(-;-) |
Alt | rs1060502684(-;-) |
Reference | Rs1060502684(TC;TC) |
Significance | Pathogenic |
Disease | Familial cancer of breast |
Variation | info |
Gene | CHEK2 |
CLNDBN | Familial cancer of breast |
Reversed | 1 |
HGVS | NC_000022.10:g.29091817_29091818delGA |
CLNSRC | |
CLNACC | RCV000469025.1, |