rs79575641
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs79575641(G;G) |
Make rs79575641(G;T) |
Make rs79575641(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 112753713 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs79575641 |
dbSNP (classic) | rs79575641 |
ClinGen | rs79575641 |
ebi | rs79575641 |
HLI | rs79575641 |
Exac | rs79575641 |
Gnomad | rs79575641 |
Varsome | rs79575641 |
LitVar | rs79575641 |
Map | rs79575641 |
PheGenI | rs79575641 |
Biobank | rs79575641 |
1000 genomes | rs79575641 |
hgdp | rs79575641 |
ensembl | rs79575641 |
geneview | rs79575641 |
scholar | rs79575641 |
rs79575641 | |
pharmgkb | rs79575641 |
gwascentral | rs79575641 |
openSNP | rs79575641 |
23andMe | rs79575641 |
SNPshot | rs79575641 |
SNPdbe | rs79575641 |
MSV3d | rs79575641 |
GWAS Ctlg | rs79575641 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs79575641(T;T) |
Alt | rs79575641(T;T) |
Reference | rs79575641(G;G) |
Significance | Other |
Disease | Familial colorectal cancer |
Variation | info |
Gene | APC |
CLNDBN | Familial colorectal cancer |
Reversed | 0 |
HGVS | NC_000005.9:g.112089410G>T |
CLNSRC | |
CLNACC | RCV000073351.1, |