Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6430538
rs6430538
CCNT2-AS1
0.925 0.080 2 134782397 intron variant C/T snv 0.62
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.830 1.000 1 2012 2019
dbSNP: rs6710823
rs6710823
CCNT2-AS1
1.000 0.040 2 134834811 intron variant G/A snv 0.23
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.800 1.000 2 2011 2012