Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5860563
ADH4 ; LOC100507053
1.000 0.080 4 99126006 intron variant -/A delins 3
rs58598658
KLF12
0.925 0.080 13 73887725 intron variant -/A;AA delins 4
rs141424017 1.000 0.080 7 115311376 intergenic variant -/CAA ins 3
rs143894582
PTPN11
1.000 0.080 12 112469070 intron variant A/-;AA delins 3
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs1042173
SLC6A4
0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs11568817
HTR1B ; LOC105377864
0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 8
rs3743832
C16orf72
1.000 0.080 16 9120023 3 prime UTR variant A/C snv 0.55 4
rs1709819
KCNJ6
1.000 0.080 21 37663813 intron variant A/C snv 0.59 3
rs1709820
KCNJ6
1.000 0.080 21 37663669 intron variant A/C snv 0.57 3
rs1787396
KCNJ6
1.000 0.080 21 37664185 intron variant A/C snv 0.57 3
rs1787398
KCNJ6
1.000 0.080 21 37665202 intron variant A/C snv 0.57 3
rs2835836
KCNJ6
1.000 0.080 21 37616885 3 prime UTR variant A/C snv 0.26 3
rs4384980 1.000 0.080 3 182741281 upstream gene variant A/C snv 0.48 1
rs7183893
LINC02694
1.000 0.080 15 38704780 intron variant A/C snv 0.23 1
rs29230
GABBR1
0.807 0.440 6 29608616 missense variant A/C;G snv 4.1E-06; 0.18 6
rs6691840
GRIK3
0.827 0.120 1 36859876 missense variant A/C;G snv 0.27; 9.2E-05 5
rs17028615
LOC100507053 ; ADH4
1.000 0.080 4 99150767 intron variant A/C;G snv 4
rs1709835
KCNJ6
1.000 0.080 21 37665334 intron variant A/C;G snv 0.57 3
rs1787404
KCNJ6
1.000 0.080 21 37677060 intron variant A/C;G snv 3
rs9378160
MICB
1.000 0.080 6 31500215 intron variant A/C;G snv 3
rs3752482
CPNE5
0.925 0.160 6 36765293 intron variant A/C;G snv 4.0E-06; 0.12 2
rs637547
NKAIN2
1.000 0.080 6 124589242 intron variant A/C;G snv 1
rs735668
TACR1
1.000 0.080 2 75135918 intron variant A/C;G snv 1
rs1332184
MIR31HG
1.000 0.080 9 21504204 intron variant A/C;G;T snv 1