rs4709583
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs4709583(A;G) |
Make rs4709583(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 6 |
Position | 162201272 |
Gene | PARK2 |
is a | snp |
is | mentioned by |
dbSNP | rs4709583 |
dbSNP (classic) | rs4709583 |
ClinGen | rs4709583 |
ebi | rs4709583 |
HLI | rs4709583 |
Exac | rs4709583 |
Gnomad | rs4709583 |
Varsome | rs4709583 |
LitVar | rs4709583 |
Map | rs4709583 |
PheGenI | rs4709583 |
Biobank | rs4709583 |
1000 genomes | rs4709583 |
hgdp | rs4709583 |
ensembl | rs4709583 |
geneview | rs4709583 |
scholar | rs4709583 |
rs4709583 | |
pharmgkb | rs4709583 |
gwascentral | rs4709583 |
openSNP | rs4709583 |
23andMe | rs4709583 |
SNPshot | rs4709583 |
SNPdbe | rs4709583 |
MSV3d | rs4709583 |
GWAS Ctlg | rs4709583 |
Max Magnitude | 0 |
[PMID 24861865] Genetic variants in apoptosis-related genes associated with colorectal hyperplasia
ClinVar | |
---|---|
Risk | rs4709583(G;G) |
Alt | rs4709583(G;G) |
Reference | Rs4709583(A;A) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | PARK2 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000006.11:g.162622304A>G |
CLNSRC | |
CLNACC | RCV000249119.1, |