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: rs102275
rs102275
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs174529
rs174529
11 61776489 intron variant T/C snv 0.34
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2018 2018
dbSNP: rs174533
rs174533
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2017 2017
dbSNP: rs174535
rs174535
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement
0.700 1.000 1 2012 2012