rs75168477
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs75168477(A;A) |
Make rs75168477(A;C) |
Make rs75168477(C;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 112727927 |
Gene | APC |
is a | snp |
is | mentioned by |
dbSNP | rs75168477 |
dbSNP (classic) | rs75168477 |
ClinGen | rs75168477 |
ebi | rs75168477 |
HLI | rs75168477 |
Exac | rs75168477 |
Gnomad | rs75168477 |
Varsome | rs75168477 |
LitVar | rs75168477 |
Map | rs75168477 |
PheGenI | rs75168477 |
Biobank | rs75168477 |
1000 genomes | rs75168477 |
hgdp | rs75168477 |
ensembl | rs75168477 |
geneview | rs75168477 |
scholar | rs75168477 |
rs75168477 | |
pharmgkb | rs75168477 |
gwascentral | rs75168477 |
openSNP | rs75168477 |
23andMe | rs75168477 |
SNPshot | rs75168477 |
SNPdbe | rs75168477 |
MSV3d | rs75168477 |
GWAS Ctlg | rs75168477 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs75168477(C;C) |
Alt | rs75168477(C;C) |
Reference | rs75168477(A;A) |
Significance | Other |
Disease | Familial colorectal cancer |
Variation | info |
Gene | APC |
CLNDBN | Familial colorectal cancer |
Reversed | 0 |
HGVS | NC_000005.9:g.112063624A>C |
CLNSRC | |
CLNACC | RCV000073686.1, |