rs863225309
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs863225309(C;T) |
Make rs863225309(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 5 |
Position | 112819329 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs863225309 |
dbSNP (classic) | rs863225309 |
ClinGen | rs863225309 |
ebi | rs863225309 |
HLI | rs863225309 |
Exac | rs863225309 |
Gnomad | rs863225309 |
Varsome | rs863225309 |
LitVar | rs863225309 |
Map | rs863225309 |
PheGenI | rs863225309 |
Biobank | rs863225309 |
1000 genomes | rs863225309 |
hgdp | rs863225309 |
ensembl | rs863225309 |
geneview | rs863225309 |
scholar | rs863225309 |
rs863225309 | |
pharmgkb | rs863225309 |
gwascentral | rs863225309 |
openSNP | rs863225309 |
23andMe | rs863225309 |
SNPshot | rs863225309 |
SNPdbe | rs863225309 |
MSV3d | rs863225309 |
GWAS Ctlg | rs863225309 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863225309(T;T) |
Alt | rs863225309(T;T) |
Reference | Rs863225309(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | APC |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000005.9:g.112155026C>T |
CLNSRC | |
CLNACC | RCV000202128.1, |