rs191486604
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs191486604(A;A) |
Make rs191486604(A;G) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 6 |
Position | 161350208 |
Gene | PARK2 |
is a | snp |
is | mentioned by |
dbSNP | rs191486604 |
dbSNP (classic) | rs191486604 |
ClinGen | rs191486604 |
ebi | rs191486604 |
HLI | rs191486604 |
Exac | rs191486604 |
Gnomad | rs191486604 |
Varsome | rs191486604 |
LitVar | rs191486604 |
Map | rs191486604 |
PheGenI | rs191486604 |
Biobank | rs191486604 |
1000 genomes | rs191486604 |
hgdp | rs191486604 |
ensembl | rs191486604 |
geneview | rs191486604 |
scholar | rs191486604 |
rs191486604 | |
pharmgkb | rs191486604 |
gwascentral | rs191486604 |
openSNP | rs191486604 |
23andMe | rs191486604 |
SNPshot | rs191486604 |
SNPdbe | rs191486604 |
MSV3d | rs191486604 |
GWAS Ctlg | rs191486604 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs191486604(A;A) |
Alt | rs191486604(A;A) |
Reference | Rs191486604(G;G) |
Significance | Probable-Pathogenic |
Disease | Parkinson Disease |
Variation | info |
Gene | PARK2 |
CLNDBN | Parkinson Disease, Juvenile |
Reversed | 1 |
HGVS | NC_000006.11:g.161771240C>T |
CLNSRC | Illumina |
CLNACC | RCV000269607.1, |