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: rs2043948
rs2043948
LTBP2
1.000 0.080 14 74606345 intron variant C/T snv 0.11
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.700 1.000 1 2011 2011
dbSNP: rs2286412
rs2286412
LTBP2
1.000 0.080 14 74502464 intron variant C/T snv 0.35
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.700 1.000 1 2011 2011
dbSNP: rs862034
rs862034
LTBP2
14 74524043 intron variant A/G snv 0.65
CUI: C0489786
Disease: Height
Height 		0.700 1.000 1 2010 2010