Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763802417
NOX1
0.882 0.040 X 100862805 missense variant G/A snv 5.9E-06 5
rs5031002
AR
1.000 0.040 X 67722783 intron variant G/A snv 1.5E-02 1.5E-02 3
rs16999497 0.925 0.040 X 129601222 regulatory region variant T/C snv 7.8E-02 2
rs5943057
CHRDL1
1.000 0.040 X 110695977 intron variant T/G snv 0.50 1
rs755622
MIF-AS1 ; MIF
0.611 0.720 22 23894205 intron variant G/C snv 0.26 44
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs4818
COMT ; MIR4761
0.683 0.440 22 19963684 synonymous variant C/G;T snv 0.34 27
rs1065852
NDUFA6-DT ; LOC112268294 ; CYP2D6
0.695 0.360 22 42130692 missense variant G/A snv 0.21 0.19 19
rs1465444723
TCN2
0.827 0.240 22 30610886 missense variant A/G snv 4.0E-06 5
rs133049
MRTFA
0.882 0.080 22 40635351 intron variant A/- delins 0.82 4
rs7291467
LGALS2
0.851 0.160 22 37576621 intron variant G/A snv 0.49 4
rs12165908
TBX1
1.000 0.040 22 19777658 intron variant G/C snv 0.20 1
rs75680863
TCN2
1.000 0.040 22 30611036 missense variant A/G;T snv 2.7E-03 1
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs1202989817
SOD1 ; LOC102724449
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs121964962
CBS
0.827 0.200 21 43062988 missense variant C/T snv 1.6E-04 5
rs9982601 0.851 0.080 21 34226827 intron variant C/T snv 0.15 4
rs2254638
N6AMT1
0.882 0.040 21 28883961 intron variant A/C;G snv 3
rs428785
ADAMTS1
0.882 0.040 21 26844276 missense variant C/A;G;T snv 1.3E-05; 0.70 0.78 3
rs771748290
CBS
0.882 0.160 21 43072114 missense variant C/A;T snv 8.1E-06; 8.1E-06 3
rs779011920
CBS
0.882 0.160 21 43066299 missense variant C/T snv 8.0E-06 3
rs143081213
RCAN1
1.000 0.040 21 34615168 upstream gene variant G/A snv 2.6E-02 2