rs786203024
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AATGTATAAGCTCCGC;AATGTATAAGCTCCGC) | 0 | common in clinvar |
Make rs786203024(-;-) |
Make rs786203024(-;TATAAGCTCCGCAATG) |
Make rs786203024(TATAAGCTCCGCAATG;TATAAGCTCCGCAATG) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 5 |
Position | 112841720 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs786203024 |
dbSNP (classic) | rs786203024 |
ClinGen | rs786203024 |
ebi | rs786203024 |
HLI | rs786203024 |
Exac | rs786203024 |
Gnomad | rs786203024 |
Varsome | rs786203024 |
LitVar | rs786203024 |
Map | rs786203024 |
PheGenI | rs786203024 |
Biobank | rs786203024 |
1000 genomes | rs786203024 |
hgdp | rs786203024 |
ensembl | rs786203024 |
geneview | rs786203024 |
scholar | rs786203024 |
rs786203024 | |
pharmgkb | rs786203024 |
gwascentral | rs786203024 |
openSNP | rs786203024 |
23andMe | rs786203024 |
SNPshot | rs786203024 |
SNPdbe | rs786203024 |
MSV3d | rs786203024 |
GWAS Ctlg | rs786203024 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786203024(-;-) |
Alt | rs786203024(-;-) |
Reference | Rs786203024(AATGTATAAGCTCCGC;AATGTATAAGCTCCGC) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | APC |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.112177417_112177432del16 |
CLNSRC | |
CLNACC | RCV000166146.1, |