Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs41467651
ND4L ; ND4 ; COX3 ; ND3
0.925 0.080 MT 10310 synonymous variant G/A snv 2
rs8126
TNFAIP2
0.807 0.080 14 103137232 3 prime UTR variant C/T snv 0.63 8
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs861528
XRCC3 ; ZFYVE21
0.925 0.080 14 103716661 intron variant C/T snv 0.17 2
rs2853826
ND4L ; COX3 ; ND5 ; ND3 ; ND4
0.925 0.080 MT 10398 missense variant A/G snv 2
rs28358278
ND3 ; ND4L ; ND5 ; COX3 ; ND4
0.925 0.080 MT 10400 synonymous variant C/T snv 2
rs12615966 0.882 0.080 2 104762499 upstream gene variant C/T snv 0.14 3
rs1130233
AKT1
0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs111638916
PSMD10
0.925 0.080 X 108084839 3 prime UTR variant G/A snv 3
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs1279599
AMD1
0.925 0.080 6 110879025 intron variant G/A snv 0.87 2
rs7768897
AMD1
0.925 0.080 6 110891080 non coding transcript exon variant A/G;T snv 2
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs201745983
ALDH2
0.752 0.200 12 111783219 missense variant G/A snv 6.8E-05 7.7E-05 14
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs16941667
ALDH2
0.925 0.080 12 111806609 intron variant C/T snv 8.6E-02 2
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 18
rs1064261
MTOR
0.925 0.080 1 11228701 missense variant G/A;T snv 0.75; 4.0E-06 3
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs2301756
PTPN11
0.851 0.120 12 112452972 intron variant A/G snv 0.21 4
rs6968084
IFRD1
0.925 0.080 7 112457066 missense variant C/T snv 0.17 0.16 2
rs3807213
IFRD1
0.882 0.200 7 112465699 intron variant G/T snv 0.57 3
rs12229892
PTPN11
0.807 0.240 12 112485589 intron variant G/A snv 1.4E-02 6
rs2295080
MTOR
0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20