Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11915160
SOX2 ; SOX2-OT
0.851 0.200 3 181713783 3 prime UTR variant C/A snv 0.11 5
rs17446614
FOXO1
0.851 0.240 13 40565740 intron variant G/A snv 0.16 5
rs3818292
SIRT1
0.827 0.280 10 67907144 intron variant A/G snv 7.1E-02 5
rs710218
SLC2A1-AS1
0.882 0.280 1 42961547 intron variant T/A snv 0.38 5
rs7211818
RPTOR
0.827 0.200 17 80715103 intron variant A/G snv 0.23 5
rs7212142
RPTOR
0.827 0.200 17 80650141 intron variant G/A snv 0.50 5
rs805304
CLIC1 ; DDAH2
0.851 0.240 6 31730311 5 prime UTR variant T/G snv 0.48 5
rs852426
ACTB
0.882 0.240 7 5526722 downstream gene variant C/T snv 0.39 5
rs1143770
MIRLET7A2 ; MIR100HG
0.882 0.200 11 122146890 intron variant C/T snv 0.53 4
rs2779248
NOS2
0.882 0.160 17 27800806 intron variant T/C snv 0.39 4
rs56094641
FTO
0.925 0.160 16 53772541 intron variant A/G;T snv 4
rs743507
NOS3
0.882 0.200 7 151010400 intron variant C/T snv 0.77 4
rs75444904
HPR ; TXNL4B
0.851 0.160 16 72061751 intron variant A/C snv 2.4E-02 4
rs7588550
ERBB4
0.851 0.160 2 212304043 intron variant G/A snv 0.96 4
rs841853
SLC2A1
0.882 0.200 1 42935767 intron variant A/C snv 0.66 4
rs117897666
LOC105370892
0.882 0.160 15 73811619 intergenic variant C/T snv 3
rs12449782 0.925 0.200 17 63498888 intron variant G/A snv 0.41 3
rs136161
APOL1
0.925 0.160 22 36261386 intron variant G/C snv 0.51 3
rs1400094618
MOK
0.882 0.240 14 102229508 missense variant A/G snv 3
rs1411766
LOC101927627
0.882 0.160 13 109599813 intron variant G/A;T snv 3
rs1567438
LPAL2
0.925 0.200 6 160458599 intron variant T/C snv 0.25 3
rs16835198 0.882 0.200 1 32861080 downstream gene variant G/T snv 0.29 3
rs2120243
VEPH1
0.925 0.200 3 157429779 intron variant A/C snv 0.59 3
rs34713741
SELENOS
0.882 0.280 15 101277671 upstream gene variant C/A;T snv 0.24 3
rs4311
ACE
0.882 0.200 17 63483402 intron variant T/C snv 0.60 3