Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7120118
rs7120118
0.716 0.360 11 47264739 intron variant T/C snv 0.38
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 2 2009 2012
dbSNP: rs2279238
rs2279238
0.790 0.320 11 47260473 missense variant C/T snv 0.26 0.26
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement
0.700 1.000 1 2012 2012