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: rs1260326
rs1260326
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 10 2010 2019
dbSNP: rs780093
rs780093
0.763 0.240 2 27519736 intron variant T/C snv 0.68
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2012 2019
dbSNP: rs780094
rs780094
0.658 0.400 2 27518370 intron variant T/C snv 0.67
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 4 2012 2019
dbSNP: rs780092
rs780092
0.827 0.160 2 27520287 intron variant A/G snv 0.18
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.800 1.000 2 2013 2017
dbSNP: rs780090
rs780090
0.925 0.120 2 27495607 upstream gene variant T/C;G snv
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs814295
rs814295
0.925 0.120 2 27520348 intron variant A/G snv 0.18
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012