rs3219487
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common genotype |
Make rs3219487(A;A) |
Make rs3219487(A;G) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 1 |
Position | 45332883 |
Gene | MUTYH |
is a | snp |
is | mentioned by |
dbSNP | rs3219487 |
dbSNP (classic) | rs3219487 |
ClinGen | rs3219487 |
ebi | rs3219487 |
HLI | rs3219487 |
Exac | rs3219487 |
Gnomad | rs3219487 |
Varsome | rs3219487 |
LitVar | rs3219487 |
Map | rs3219487 |
PheGenI | rs3219487 |
Biobank | rs3219487 |
1000 genomes | rs3219487 |
hgdp | rs3219487 |
ensembl | rs3219487 |
geneview | rs3219487 |
scholar | rs3219487 |
rs3219487 | |
pharmgkb | rs3219487 |
gwascentral | rs3219487 |
openSNP | rs3219487 |
23andMe | rs3219487 |
SNPshot | rs3219487 |
SNPdbe | rs3219487 |
MSV3d | rs3219487 |
GWAS Ctlg | rs3219487 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 30218772] An Intronic Single Nucleotide Polymorphism in the MUTYH Gene Is Associated with Increased Risk for HCV-induced Hepatocellular carcinoma.