Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs386352319
KCNJ5
0.827 0.080 11 128911724 missense variant G/A;C snv 8
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs121912535
STON1-GTF2A1L ; LHCGR ; GTF2A1L
0.827 0.240 2 48688427 missense variant A/C snv 6
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs121908874
TSHR ; LOC101928462
0.807 0.080 14 81143584 missense variant T/C snv 7
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 11
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs5277
PACERR ; PTGS2
0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 9
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs4925386
LAMA5
0.776 0.080 20 62345988 intron variant T/C snv 0.56 14
rs121912532
STON1-GTF2A1L ; LHCGR ; GTF2A1L
0.776 0.280 2 48688065 missense variant C/A;G;T snv 1.2E-05 12
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
rs3842787
PTGS1
0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 11
rs1060503115
PMS2
0.763 0.400 7 5978664 missense variant T/A;G snv 13
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 14
rs7873784
TLR4
0.752 0.440 9 117716658 3 prime UTR variant G/A;C;T snv 11
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 16
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs770460061
GSTP1
0.742 0.240 11 67585239 missense variant T/C;G snv 4.0E-06; 1.2E-05 14
rs150766139
NTHL1 ; TSC2
0.742 0.320 16 2046238 stop gained G/A snv 1.4E-03 1.4E-03 13
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 17
rs1042821
MSH6
0.732 0.280 2 47783349 missense variant G/A;C;T snv 0.18; 8.6E-06 16
rs536562413
FBXO11 ; MSH6
0.732 0.240 2 47799934 missense variant A/G snv 1.2E-05 7.0E-06 15
rs10795668
LOC105376400
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 17