Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs2229616
MC4R
0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 22
rs800629
LOC107985869
0.882 0.120 2 37752757 intergenic variant G/A snv 3
rs4353747 1.000 0.040 22 30630488 downstream gene variant C/A;T snv 1
rs6756667
EPAS1
1.000 0.040 2 46352270 intron variant A/G snv 0.62 1
rs6520015
LOC642648 ; MIRLET7BHG
1.000 0.040 22 46067551 non coding transcript exon variant T/A;C snv 1
rs4253747
PPARA
1.000 0.040 22 46217340 intron variant T/A snv 0.30 1
rs7292407
PRR34-AS1 ; MIRLET7BHG
1.000 0.040 22 46057832 non coding transcript exon variant C/A;T snv 1