Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1017418
LOC730100
1.000 0.080 2 51821024 intron variant G/A;C snv 1
rs10496768
THSD7B
1.000 0.080 2 137322384 intron variant G/A snv 9.5E-02 1
rs1869324
THSD7B
1.000 0.080 2 137469872 intron variant G/A snv 7.9E-02 1
rs6715729
TACR1 ; LOC105374811
1.000 0.080 2 75198602 synonymous variant A/G snv 0.48 0.58 1
rs735668
TACR1
1.000 0.080 2 75135918 intron variant A/C;G snv 1
rs7597960 1.000 0.080 2 122667075 intron variant A/G;T snv 1
rs7607774 1.000 0.080 2 236520511 intergenic variant G/A snv 7.4E-02 1
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs2002594
FAM162A
1.000 0.080 3 122392714 intron variant A/G snv 0.59 3
rs2168784 1.000 0.080 3 164872151 intergenic variant C/T snv 0.24 3
rs6777876 1.000 0.080 3 11915124 upstream gene variant A/G snv 9.9E-02 3
rs2134655
DRD3
0.925 0.080 3 114139354 intron variant C/A;T snv 2
rs2727943 0.925 0.080 3 1856289 intergenic variant T/A;C snv 2
rs11922615
SETD5
1.000 0.080 3 9416623 intron variant A/G snv 8.4E-02 1
rs12489456
SLC6A6
1.000 0.080 3 14459666 intron variant G/A;T snv 1
rs3773165
SLC6A6
1.000 0.080 3 14482762 intron variant G/A snv 0.20 1
rs4384980 1.000 0.080 3 182741281 upstream gene variant A/C snv 0.48 1
rs6443238
SETD5
1.000 0.080 3 9407371 intron variant C/T snv 8.4E-02 1
rs6778524
PLCL2
1.000 0.080 3 16814451 intron variant T/C snv 8.3E-02 1
rs9847462 1.000 0.080 3 164840807 intergenic variant A/G snv 0.14 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs1693482
ADH1C ; ADH1B
0.807 0.240 4 99342808 missense variant C/T snv 0.34 0.31 12
rs35385902
ADH1C ; ADH1B
0.807 0.240 4 99347122 missense variant C/A;T snv 2.0E-05; 1.1E-03 9