Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs758272654
GNAS
0.611 0.680 20 58909201 synonymous variant T/C snv 4.0E-06 7.0E-06 50
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs225014
DIO2
0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs2057482
HIF1A-AS2 ; HIF1A-AS3 ; HIF1A
0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs679620
MMP3
0.716 0.360 11 102842889 missense variant T/C snv 0.58 0.57 17
rs2695121
NR1H2
0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs6198
NR3C1
0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs34598529
HBB
0.724 0.280 11 5227100 5 prime UTR variant T/C snv 8.9E-04 14
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs806368
CNR1
0.752 0.280 6 88140381 3 prime UTR variant T/C snv 0.19 14
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs562962093
MBL2
0.742 0.520 10 52771740 upstream gene variant T/C snv 7.0E-06 13
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs12218
SAA1
0.763 0.280 11 18269774 synonymous variant T/C snv 0.42 0.36 11
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11