rs2952615
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2952615(C;C) |
Make rs2952615(C;G) |
Make rs2952615(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 112803191 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs2952615 |
dbSNP (classic) | rs2952615 |
ClinGen | rs2952615 |
ebi | rs2952615 |
HLI | rs2952615 |
Exac | rs2952615 |
Gnomad | rs2952615 |
Varsome | rs2952615 |
LitVar | rs2952615 |
Map | rs2952615 |
PheGenI | rs2952615 |
Biobank | rs2952615 |
1000 genomes | rs2952615 |
hgdp | rs2952615 |
ensembl | rs2952615 |
geneview | rs2952615 |
scholar | rs2952615 |
rs2952615 | |
pharmgkb | rs2952615 |
gwascentral | rs2952615 |
openSNP | rs2952615 |
23andMe | rs2952615 |
SNPshot | rs2952615 |
SNPdbe | rs2952615 |
MSV3d | rs2952615 |
GWAS Ctlg | rs2952615 |
Max Magnitude | 0 |
? | (C;C) (C;G) (G;G) | 28 |
---|---|---|
|
ClinVar | |
---|---|
Risk | rs2952615(G;G) |
Alt | rs2952615(G;G) |
Reference | rs2952615(C;C) |
Significance | Other |
Disease | Familial colorectal cancer |
Variation | info |
Gene | APC |
CLNDBN | Familial colorectal cancer |
Reversed | 1 |
HGVS | NC_000005.9:g.112138888G>C |
CLNSRC | |
CLNACC | RCV000074036.1, |