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: rs12474609
rs12474609
LRP1B
2 140963573 intron variant A/T snv 0.18
CUI: C0001811
Disease: Aging
Aging 		0.700 1.000 1 2010 2010
dbSNP: rs294588
rs294588 		5 163571509 regulatory region variant T/C snv 0.70
CUI: C0001811
Disease: Aging
Aging 		0.700 1.000 1 2013 2013
dbSNP: rs6925255
rs6925255 		6 79756407 regulatory region variant A/C;G;T snv
CUI: C0001811
Disease: Aging
Aging 		0.700 1.000 1 2013 2013
dbSNP: rs9918668
rs9918668
LOC107986820
7 94062432 intron variant G/A snv 0.47
CUI: C0001811
Disease: Aging
Aging 		0.700 1.000 1 2013 2013