Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6982636 8 125467073 intron variant G/A snv 0.43 6
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 6
rs737410
ARRB1
11 75315038 intron variant A/G snv 4.3E-02 6
rs7499892
CETP
16 56972678 intron variant C/G;T snv 6
rs760242
DHCR7
11 71435530 missense variant C/T snv 2.2E-04 6.3E-05 6
rs7993724
PDX1 ; PLUT
13 27919139 upstream gene variant T/C snv 5.6E-03 6
rs8138057
PDXP
22 37665537 intron variant G/A snv 3.0E-03 1.3E-02 6
rs9341023
ESR1
6 152062578 intron variant C/T snv 6
rs9622186 22 35377961 upstream gene variant A/G snv 3.7E-03 6
rs10199768
APOB
2 21021128 intron variant G/T snv 0.35 5
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20 5
rs11207997
DOCK7 ; ANGPTL3
1 62596235 intron variant C/T snv 0.39 5
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 5
rs11563251
UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A6 ; UGT1A5 ; UGT1A1 ; UGT1A4 ; UGT1A10 ; UGT1A8
2 233770738 3 prime UTR variant C/T snv 0.19 5
rs1167998
DOCK7
1 62465961 intron variant C/A snv 0.57 5
rs11921179
TRH
3 129976195 intron variant G/A snv 0.96 5
rs1321655
ATP1A2
1 160124668 intron variant A/G;T snv 5
rs17243641
LOC105376326 ; TRAF2 ; MIR4479
9 136886986 intron variant G/T snv 2.6E-03 5
rs1748197
DOCK7
1 62590441 intron variant G/A snv 0.42 5
rs17513478
RIPK1
6 3101321 intron variant G/A snv 5.7E-03 5
rs180327
BUD13
11 116752943 intron variant C/T snv 0.58 5
rs2072560
ZPR1 ; APOA5
11 116791110 missense variant T/C snv 0.89 0.94 5
rs2131925
DOCK7
1 62560271 intron variant G/T snv 0.57 5