rs10476823
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10476823(C;C) |
Make rs10476823(C;T) |
Make rs10476823(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 155434249 |
is a | snp |
is | mentioned by |
dbSNP | rs10476823 |
dbSNP (classic) | rs10476823 |
ClinGen | rs10476823 |
ebi | rs10476823 |
HLI | rs10476823 |
Exac | rs10476823 |
Gnomad | rs10476823 |
Varsome | rs10476823 |
LitVar | rs10476823 |
Map | rs10476823 |
PheGenI | rs10476823 |
Biobank | rs10476823 |
1000 genomes | rs10476823 |
hgdp | rs10476823 |
ensembl | rs10476823 |
geneview | rs10476823 |
scholar | rs10476823 |
rs10476823 | |
pharmgkb | rs10476823 |
gwascentral | rs10476823 |
openSNP | rs10476823 |
23andMe | rs10476823 |
SNPshot | rs10476823 |
SNPdbe | rs10476823 |
MSV3d | rs10476823 |
GWAS Ctlg | rs10476823 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 24861865] Genetic variants in apoptosis-related genes associated with colorectal hyperplasia