Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1143770
MIRLET7A2 ; MIR100HG
0.882 0.200 11 122146890 intron variant C/T snv 0.53 4
rs2075241
LRP6 ; BCL2L14
0.882 0.200 12 12138545 intron variant G/A;C snv 0.18 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
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
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
rs2120243
VEPH1
0.925 0.200 3 157429779 intron variant A/C snv 0.59 3
rs2234694
SOD1
0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02 3
rs2281999
UNC13B
0.925 0.160 9 35381507 intron variant C/T snv 0.35 0.38 3
rs2305619
VEPH1 ; PTX3
0.882 0.240 3 157437072 intron variant A/G snv 0.55 0.50 3
rs4311
ACE
0.882 0.200 17 63483402 intron variant T/C snv 0.60 3
rs6997279
SLC30A8
0.882 0.160 8 116961613 intron variant G/T snv 0.20 3
rs741301
ELMO1
0.925 0.160 7 36878390 intron variant C/T snv 0.59 3
rs10823108
SIRT1
0.925 0.160 10 67900736 intron variant G/A snv 7.1E-02 2
rs1326934
SORBS1
0.925 0.200 10 95524324 intron variant C/T snv 0.63 2