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: rs1572521
rs1572521
1 103097312 intron variant T/G snv 0.96
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs3753841
rs3753841
0.827 0.080 1 102914362 missense variant G/A snv 0.61 0.49
CUI: C0017612
Disease: Glaucoma, Open-Angle
Glaucoma, Open-Angle
0.700 1.000 1 2012 2012
dbSNP: rs4338381
rs4338381
1.000 0.040 1 103107371 intron variant A/C;G snv
CUI: C0489786
Disease: Height
Height
0.700 1.000 1 2011 2011