rs2298298
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs2298298(A;G) |
Make rs2298298(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 20637835 |
Gene | PINK1 |
is a | snp |
is | mentioned by |
dbSNP | rs2298298 |
dbSNP (classic) | rs2298298 |
ClinGen | rs2298298 |
ebi | rs2298298 |
HLI | rs2298298 |
Exac | rs2298298 |
Gnomad | rs2298298 |
Varsome | rs2298298 |
LitVar | rs2298298 |
Map | rs2298298 |
PheGenI | rs2298298 |
Biobank | rs2298298 |
1000 genomes | rs2298298 |
hgdp | rs2298298 |
ensembl | rs2298298 |
geneview | rs2298298 |
scholar | rs2298298 |
rs2298298 | |
pharmgkb | rs2298298 |
gwascentral | rs2298298 |
openSNP | rs2298298 |
23andMe | rs2298298 |
SNPshot | rs2298298 |
SNPdbe | rs2298298 |
MSV3d | rs2298298 |
GWAS Ctlg | rs2298298 |
GMAF | 0.1713 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
This SNP may be related to obesity and diabetes.
Genomic variants at the PINK1 locus are associated with transcript abundance and plasma nonesterified fatty acid concentrations in European whites. A allele associated with higher PINK1 transcript levels.[PMID 18495756]
ClinVar | |
---|---|
Risk | rs2298298(G;G) |
Alt | rs2298298(G;G) |
Reference | Rs2298298(A;A) |
Significance | Non-pathogenic |
Disease | not specified Parkinson Disease |
Variation | info |
Gene | PINK1 |
CLNDBN | not specified Parkinson Disease, Recessive |
Reversed | 0 |
HGVS | NC_000001.10:g.20964328A>G |
CLNSRC | |
CLNACC | RCV000254305.1, RCV000270301.1, |