Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 26
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs185847354
ADIPOQ ; ADIPOQ-AS1
0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs2431697 0.776 0.240 5 160452971 intron variant T/C snv 0.44 10
rs4251961
IL1RN
0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs6882076
TIMD4
0.827 0.160 5 156963286 upstream gene variant T/C snv 0.56 9
rs10509681
CYP2C8
0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 8
rs16847548 0.807 0.120 1 162065484 upstream gene variant T/C snv 0.22 8
rs17366743
ADIPOQ-AS1 ; ADIPOQ
0.807 0.280 3 186854300 missense variant T/C snv 2.2E-02 2.1E-02 7
rs8075977 0.827 0.160 17 1757507 upstream gene variant T/C snv 0.37 5
rs9332978
CYP4A11
0.882 0.040 1 46942278 upstream gene variant T/C snv 7.3E-02 5
rs1199475313
ADRB3
0.851 0.040 8 37966277 missense variant T/C snv 7.0E-06 4
rs1790349
DHCR7
0.882 0.040 11 71431304 intron variant T/C snv 0.19 4