rs876658868
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs876658868(C;T) |
Make rs876658868(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 112827116 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs876658868 |
dbSNP (classic) | rs876658868 |
ClinGen | rs876658868 |
ebi | rs876658868 |
HLI | rs876658868 |
Exac | rs876658868 |
Gnomad | rs876658868 |
Varsome | rs876658868 |
LitVar | rs876658868 |
Map | rs876658868 |
PheGenI | rs876658868 |
Biobank | rs876658868 |
1000 genomes | rs876658868 |
hgdp | rs876658868 |
ensembl | rs876658868 |
geneview | rs876658868 |
scholar | rs876658868 |
rs876658868 | |
pharmgkb | rs876658868 |
gwascentral | rs876658868 |
openSNP | rs876658868 |
23andMe | rs876658868 |
SNPshot | rs876658868 |
SNPdbe | rs876658868 |
MSV3d | rs876658868 |
GWAS Ctlg | rs876658868 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876658868(T;T) |
Alt | rs876658868(T;T) |
Reference | Rs876658868(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | APC |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.112162813C>T |
CLNSRC | |
CLNACC | RCV000219498.2, |