rs587780173
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs587780173(-;-) |
Make rs587780173(-;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 22 |
Position | 28695715 |
Gene | CHEK2 |
is a | snp |
is | mentioned by |
dbSNP | rs587780173 |
dbSNP (classic) | rs587780173 |
ClinGen | rs587780173 |
ebi | rs587780173 |
HLI | rs587780173 |
Exac | rs587780173 |
Gnomad | rs587780173 |
Varsome | rs587780173 |
LitVar | rs587780173 |
Map | rs587780173 |
PheGenI | rs587780173 |
Biobank | rs587780173 |
1000 genomes | rs587780173 |
hgdp | rs587780173 |
ensembl | rs587780173 |
geneview | rs587780173 |
scholar | rs587780173 |
rs587780173 | |
pharmgkb | rs587780173 |
gwascentral | rs587780173 |
openSNP | rs587780173 |
23andMe | rs587780173 |
SNPshot | rs587780173 |
SNPdbe | rs587780173 |
MSV3d | rs587780173 |
GWAS Ctlg | rs587780173 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587780173(-;-) |
Alt | rs587780173(-;-) |
Reference | Rs587780173(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CHEK2 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000022.10:g.29091703delA |
CLNSRC | |
CLNACC | RCV000115991.3, |