rs76601225
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs76601225(A;A) |
Make rs76601225(A;C) |
Make rs76601225(C;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 112811070 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs76601225 |
dbSNP (classic) | rs76601225 |
ClinGen | rs76601225 |
ebi | rs76601225 |
HLI | rs76601225 |
Exac | rs76601225 |
Gnomad | rs76601225 |
Varsome | rs76601225 |
LitVar | rs76601225 |
Map | rs76601225 |
PheGenI | rs76601225 |
Biobank | rs76601225 |
1000 genomes | rs76601225 |
hgdp | rs76601225 |
ensembl | rs76601225 |
geneview | rs76601225 |
scholar | rs76601225 |
rs76601225 | |
pharmgkb | rs76601225 |
gwascentral | rs76601225 |
openSNP | rs76601225 |
23andMe | rs76601225 |
SNPshot | rs76601225 |
SNPdbe | rs76601225 |
MSV3d | rs76601225 |
GWAS Ctlg | rs76601225 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs76601225(C;C) |
Alt | rs76601225(C;C) |
Reference | rs76601225(A;A) |
Significance | Other |
Disease | Familial colorectal cancer |
Variation | info |
Gene | APC |
CLNDBN | Familial colorectal cancer |
Reversed | 0 |
HGVS | NC_000005.9:g.112146767A>C |
CLNSRC | |
CLNACC | RCV000073532.1, |