Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs12778366
SIRT1
0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs4746720
SIRT1
0.790 0.320 10 67917073 3 prime UTR variant T/C snv 2.4E-02 7
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs2959656
MEN1 ; MAP4K2
0.851 0.160 11 64804546 missense variant T/C snv 0.94 0.90 5
rs104894190
AIP
0.882 0.120 11 67490911 missense variant G/A snv 1.7E-03 1.1E-03 4
rs3740051
SIRT1
0.925 0.200 10 67884201 upstream gene variant A/G;T snv 2
rs267606573
AIP ; MIR6752
1.000 0.120 11 67490391 stop gained A/G;T snv 3.6E-05 1
rs17083838
CDK8
1.000 0.120 13 26336975 intron variant G/A;T snv 5.4E-02 1
rs2359536
LOC105376442
1.000 0.120 10 20610679 intergenic variant T/C snv 0.31 1
rs10763170
PCDH15
1.000 0.120 10 55017264 intron variant T/C snv 0.52 1