Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7833904 0.882 0.040 8 58505103 upstream gene variant A/T snv 0.55 3
rs2227631
SERPINE1
0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs7895340
TCF7L2
0.851 0.160 10 113041766 intron variant G/A snv 0.53 4
rs9303277
IKZF3
0.790 0.240 17 39820216 intron variant C/T snv 0.52 9
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 11
rs4803455
TGFB1
0.752 0.280 19 41345604 intron variant C/A snv 0.51 11
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs20455
KIF6 ; LOC107986594
0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs243330
SOCS1 ; RMI2 ; LOC105371082
0.851 0.240 16 11257134 intron variant C/T snv 0.49 4
rs2071746
HMOX1
0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs16147
LOC107986777 ; NPY
0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 18
rs3861950
TNFSF4
0.827 0.160 1 173187153 intron variant T/C snv 0.47 7
rs4845623
IL6R
0.925 0.040 1 154443301 intron variant A/G snv 0.47 4
rs2518136
AHSG
0.851 0.120 3 186620038 intron variant T/C snv 0.46 4
rs7217186
ALOX15
0.827 0.120 17 4636097 intron variant C/T snv 0.45 5
rs213045
ECE1
0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs7439293
PALLD
0.807 0.080 4 168756335 non coding transcript exon variant G/A snv 0.44 6
rs660339
UCP2
0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98