rs17716310
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs17716310(A;A) |
Make rs17716310(A;C) |
Make rs17716310(C;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 135141069 |
Gene | C5orf66 |
is a | snp |
is | mentioned by |
dbSNP | rs17716310 |
dbSNP (classic) | rs17716310 |
ClinGen | rs17716310 |
ebi | rs17716310 |
HLI | rs17716310 |
Exac | rs17716310 |
Gnomad | rs17716310 |
Varsome | rs17716310 |
LitVar | rs17716310 |
Map | rs17716310 |
PheGenI | rs17716310 |
Biobank | rs17716310 |
1000 genomes | rs17716310 |
hgdp | rs17716310 |
ensembl | rs17716310 |
geneview | rs17716310 |
scholar | rs17716310 |
rs17716310 | |
pharmgkb | rs17716310 |
gwascentral | rs17716310 |
openSNP | rs17716310 |
23andMe | rs17716310 |
SNPshot | rs17716310 |
SNPdbe | rs17716310 |
MSV3d | rs17716310 |
GWAS Ctlg | rs17716310 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 27177089] Identification of a functional variant for colorectal cancer risk mapping to chromosome 5q31.1.