Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs9551963 0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs9925481 0.882 0.160 16 11003622 intron variant C/G;T snv 5
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs999947969 0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1337503417 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs1380959039 1.000 0.080 10 77086524 synonymous variant A/G snv 4.0E-06 2
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs5629 0.925 0.080 20 49513169 stop gained G/A;T snv 4.0E-06; 0.25 3
rs1177506410
AGT
0.776 0.240 1 230706148 missense variant G/C snv 4.0E-06 7.0E-06 12
rs771676129 0.827 0.080 7 80671082 synonymous variant C/T snv 4.0E-06 7
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs758801521 0.882 0.160 8 26770618 missense variant A/G snv 4.0E-06 4
rs1012841819 0.882 0.160 2 96115728 missense variant G/A snv 4.0E-06 4
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1384915680
TH
1.000 0.080 11 2166903 synonymous variant G/A snv 4.3E-06 2
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs1462059537 0.882 0.160 4 147535944 missense variant C/T snv 8.0E-06 4
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48