Have questions? Visit https://www.reddit.com/r/SNPedia

rs2298298

From SNPedia

Orientationplus
Stabilizedplus
Make rs2298298(A;G)
Make rs2298298(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position20637835
GenePINK1
is asnp
is mentioned by
dbSNPrs2298298
dbSNP (classic)rs2298298
ClinGenrs2298298
ebirs2298298
HLIrs2298298
Exacrs2298298
Gnomadrs2298298
Varsomers2298298
LitVarrs2298298
Maprs2298298
PheGenIrs2298298
Biobankrs2298298
1000 genomesrs2298298
hgdprs2298298
ensemblrs2298298
geneviewrs2298298
scholarrs2298298
googlers2298298
pharmgkbrs2298298
gwascentralrs2298298
openSNPrs2298298
23andMers2298298
SNPshotrs2298298
SNPdbers2298298
MSV3drs2298298
GWAS Ctlgrs2298298
GMAF0.1713
Max Magnitude0
? (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,