Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs4245739
MDM4
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 6
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs5743618
TLR1
0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 6
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 6
rs2178146 0.827 0.080 16 86430089 downstream gene variant T/C snv 0.31 5
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 5
rs4819388
ICOSLG
0.790 0.240 21 44227538 3 prime UTR variant T/C snv 5
rs11209026
IL23R
0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 5
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 4
rs667282
CHRNA5
0.790 0.120 15 78571130 intron variant T/C snv 0.28 4
rs351855
FGFR4
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 4
rs1859168
HOTTIP
0.790 0.160 7 27202740 non coding transcript exon variant A/C;G;T snv 4
rs63750623
MSH2
0.925 0.160 2 47480707 stop gained C/G;T snv 4
rs2274223
PLCE1
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 4
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 4
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 4
rs744166
STAT3
0.689 0.560 17 42362183 intron variant A/G snv 0.48 4
rs4833095
TLR1
0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 4
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 3
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 3
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 3
rs746481984
CDH1
0.851 0.120 16 68819393 missense variant C/G;T snv 4.0E-06 3