Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1108580
DBH
0.790 0.240 9 133639992 splice region variant A/G snv 0.45 0.54 9
rs4795541
SLC6A4 ; LOC105371720
0.807 0.200 17 30237299 upstream gene variant A/G snv 7
rs13273442 0.882 0.080 8 42688874 intergenic variant A/G snv 0.66 4
rs111325002 1.000 0.080 3 96134788 intergenic variant A/G snv 8.6E-03 2
rs1437134
NFAT5
1.000 0.080 16 69696523 3 prime UTR variant A/G snv 0.66 1
rs1868152 0.925 0.080 3 186502274 intergenic variant A/G;T snv 0.85 2
rs4290270
TPH2
0.724 0.320 12 72022455 synonymous variant A/T snv 0.57 0.55 17
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs6719226 1.000 0.080 2 25173143 upstream gene variant C/G snv 0.13 1
rs684513
CHRNA5
0.925 0.080 15 78566058 intron variant C/G;T snv 5
rs2005290
OR3A2
1.000 0.080 17 3284718 intron variant C/G;T snv 2
rs6989250 1.000 0.080 8 53253835 upstream gene variant C/G;T snv 1
rs1079597
DRD2
0.827 0.080 11 113425564 intron variant C/T snv 0.18 5
rs2234918
OPRD1
0.827 0.200 1 28863085 synonymous variant C/T snv 0.59 0.50 5
rs678849
OPRD1
0.882 0.120 1 28818676 intron variant C/T snv 0.44 5
rs149775276
CHRNB3
0.925 0.080 8 42732292 missense variant C/T snv 3.6E-04 4.9E-04 2
rs150954431
NCOR2
1.000 0.080 12 124517777 intron variant C/T snv 1.6E-02 2
rs6871510
HOMER1
1.000 0.080 5 79496521 intron variant C/T snv 0.22 1
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs2235749
PDYN-AS1 ; PDYN
0.790 0.200 20 1979293 3 prime UTR variant G/A snv 0.37 7
rs10052957
NR3C1
0.851 0.160 5 143407136 non coding transcript exon variant G/A snv 0.28 4
rs779838446
CHRNA6
0.925 0.080 8 42756217 missense variant G/A snv 4.0E-06 7.0E-06 2
rs2229163
CHRM4
1.000 0.080 11 46385307 synonymous variant G/A snv 1.0E-02 3.9E-02 1