rs5934683
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs5934683(C;C) |
Make rs5934683(C;T) |
Make rs5934683(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | X |
Position | 9783434 |
is a | snp |
is | mentioned by |
dbSNP | rs5934683 |
dbSNP (classic) | rs5934683 |
ClinGen | rs5934683 |
ebi | rs5934683 |
HLI | rs5934683 |
Exac | rs5934683 |
Gnomad | rs5934683 |
Varsome | rs5934683 |
LitVar | rs5934683 |
Map | rs5934683 |
PheGenI | rs5934683 |
Biobank | rs5934683 |
1000 genomes | rs5934683 |
hgdp | rs5934683 |
ensembl | rs5934683 |
geneview | rs5934683 |
scholar | rs5934683 |
rs5934683 | |
pharmgkb | rs5934683 |
gwascentral | rs5934683 |
openSNP | rs5934683 |
23andMe | rs5934683 |
SNPshot | rs5934683 |
SNPdbe | rs5934683 |
MSV3d | rs5934683 |
GWAS Ctlg | rs5934683 |
GMAF | 0.3736 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 22634755![]() |
Trait | |
Title | Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk. |
Risk Allele | |
P-val | 7E-10 |
Odds Ratio | 1.0700 None |