rs786201856
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs786201856(C;T) |
Make rs786201856(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 5 |
Position | 112815507 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs786201856 |
dbSNP (classic) | rs786201856 |
ClinGen | rs786201856 |
ebi | rs786201856 |
HLI | rs786201856 |
Exac | rs786201856 |
Gnomad | rs786201856 |
Varsome | rs786201856 |
LitVar | rs786201856 |
Map | rs786201856 |
PheGenI | rs786201856 |
Biobank | rs786201856 |
1000 genomes | rs786201856 |
hgdp | rs786201856 |
ensembl | rs786201856 |
geneview | rs786201856 |
scholar | rs786201856 |
rs786201856 | |
pharmgkb | rs786201856 |
gwascentral | rs786201856 |
openSNP | rs786201856 |
23andMe | rs786201856 |
SNPshot | rs786201856 |
SNPdbe | rs786201856 |
MSV3d | rs786201856 |
GWAS Ctlg | rs786201856 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786201856(T;T) |
Alt | rs786201856(T;T) |
Reference | Rs786201856(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1 |
Variation | info |
Gene | APC |
CLNDBN | Hereditary cancer-predisposing syndrome not provided Familial adenomatous polyposis 1 |
Reversed | 0 |
HGVS | NC_000005.9:g.112151204C>T |
CLNSRC | |
CLNACC | RCV000164351.2, RCV000202113.1, RCV000226000.2, |