rs786204169
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;T) | 6.5 | Familial Adenomatous Polyposis |
(T;T) | 0 | common in clinvar |
Make rs786204169(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 5 |
Position | 112839424 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs786204169 |
dbSNP (classic) | rs786204169 |
ClinGen | rs786204169 |
ebi | rs786204169 |
HLI | rs786204169 |
Exac | rs786204169 |
Gnomad | rs786204169 |
Varsome | rs786204169 |
LitVar | rs786204169 |
Map | rs786204169 |
PheGenI | rs786204169 |
Biobank | rs786204169 |
1000 genomes | rs786204169 |
hgdp | rs786204169 |
ensembl | rs786204169 |
geneview | rs786204169 |
scholar | rs786204169 |
rs786204169 | |
pharmgkb | rs786204169 |
gwascentral | rs786204169 |
openSNP | rs786204169 |
23andMe | rs786204169 |
SNPshot | rs786204169 |
SNPdbe | rs786204169 |
MSV3d | rs786204169 |
GWAS Ctlg | rs786204169 |
Max Magnitude | 6.5 |
ClinVar | |
---|---|
Risk | rs786204169(G;G) |
Alt | rs786204169(G;G) |
Reference | Rs786204169(T;T) |
Significance | Pathogenic |
Disease | Familial adenomatous polyposis 1 |
Variation | info |
Gene | APC |
CLNDBN | Familial adenomatous polyposis 1 |
Reversed | 0 |
HGVS | NC_000005.9:g.112175121T>G |
CLNSRC | |
CLNACC | RCV000168191.2, |