rs964293
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs964293(G;G) |
Make rs964293(G;T) |
Make rs964293(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 20 |
Position | 54200178 |
is a | snp |
is | mentioned by |
dbSNP | rs964293 |
dbSNP (classic) | rs964293 |
ClinGen | rs964293 |
ebi | rs964293 |
HLI | rs964293 |
Exac | rs964293 |
Gnomad | rs964293 |
Varsome | rs964293 |
LitVar | rs964293 |
Map | rs964293 |
PheGenI | rs964293 |
Biobank | rs964293 |
1000 genomes | rs964293 |
hgdp | rs964293 |
ensembl | rs964293 |
geneview | rs964293 |
scholar | rs964293 |
rs964293 | |
pharmgkb | rs964293 |
gwascentral | rs964293 |
openSNP | rs964293 |
23andMe | rs964293 |
SNPshot | rs964293 |
SNPdbe | rs964293 |
MSV3d | rs964293 |
GWAS Ctlg | rs964293 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 26766742] CYP24A1 variant rs964293 modifies the association between use of combination hormone replacement therapy and colorectal cancer risk.