rs786201134
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs786201134(-;-) |
Make rs786201134(-;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 5 |
Position | 112841351 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs786201134 |
dbSNP (classic) | rs786201134 |
ClinGen | rs786201134 |
ebi | rs786201134 |
HLI | rs786201134 |
Exac | rs786201134 |
Gnomad | rs786201134 |
Varsome | rs786201134 |
LitVar | rs786201134 |
Map | rs786201134 |
PheGenI | rs786201134 |
Biobank | rs786201134 |
1000 genomes | rs786201134 |
hgdp | rs786201134 |
ensembl | rs786201134 |
geneview | rs786201134 |
scholar | rs786201134 |
rs786201134 | |
pharmgkb | rs786201134 |
gwascentral | rs786201134 |
openSNP | rs786201134 |
23andMe | rs786201134 |
SNPshot | rs786201134 |
SNPdbe | rs786201134 |
MSV3d | rs786201134 |
GWAS Ctlg | rs786201134 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786201134(-;-) |
Alt | rs786201134(-;-) |
Reference | Rs786201134(T;T) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | APC |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.112177048delT |
CLNSRC | |
CLNACC | RCV000162741.1, |