Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35381288
ADRB3
8 37965106 non coding transcript exon variant C/G snv 7.4E-03 6
rs35980686
MIR8085 ; BCL3
19 44757093 missense variant T/C snv 1.1E-03 4.4E-03 6
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs4251583
IRAK4
12 43783705 missense variant A/G snv 8.6E-04 1.1E-03 6
rs5176
LRP8
1 53246137 3 prime UTR variant T/G snv 6.4E-04 6
rs533617
APOB
2 21011100 missense variant T/C snv 3.1E-02 2.9E-02 6
rs583104 1 109278685 downstream gene variant G/T snv 0.63 6
rs660240
CELSR2
1 109275216 3 prime UTR variant T/C snv 0.75 6
rs737410
ARRB1
11 75315038 intron variant A/G snv 4.3E-02 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
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 5
rs10789117
DOCK7 ; ANGPTL3
1 62606594 intron variant A/C;T snv 5
rs11563251
UGT1A9 ; UGT1A7 ; UGT1A3 ; UGT1A6 ; UGT1A5 ; UGT1A1 ; UGT1A4 ; UGT1A10 ; UGT1A8
2 233770738 3 prime UTR variant C/T snv 0.19 5
rs11828157
MMP13
11 102947395 intron variant G/A snv 4.7E-02 5
rs11921179
TRH
3 129976195 intron variant G/A snv 0.96 5
rs1321655
ATP1A2
1 160124668 intron variant A/G;T snv 5
rs1456649
FMN2
1 240288305 intron variant G/C snv 3.0E-03 5
rs16880248
CNR1
6 88141968 3 prime UTR variant G/T snv 2.7E-02 5
rs17243641
LOC105376326 ; TRAF2 ; MIR4479
9 136886986 intron variant G/T snv 2.6E-03 5