Source: GWASCAT

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: rs1009360
rs1009360
2 65048915 intron variant T/C snv 0.51
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2018 2018
dbSNP: rs1009360
rs1009360
2 65048915 intron variant T/C snv 0.51
High density lipoprotein measurement
0.700 1.000 1 2018 2018