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: rs228769
rs228769
HDAC5 ; LOC105371789
17 44115817 intron variant G/A;C snv
CUI: C0005938
Disease: Bone Density
Bone Density 		0.800 1.000 1 2009 2009
dbSNP: rs453789
rs453789
HDAC5 ; LOC105371789
17 44118647 intron variant A/C snv 0.97
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2012 2012