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: rs653178
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.710 1.000 1 2011 2013