Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2509843 11 98254676 intergenic variant A/C;G;T snv 2
rs2155907 11 98223945 intergenic variant C/T snv 0.38 2
rs945032
BDKRB2
0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 5
rs1133503
MANEA
1.000 0.040 6 95606712 3 prime UTR variant C/G;T snv 4
rs12745968
DIPK1A
1 92936280 intron variant A/G snv 0.36 2
rs11164835
DIPK1A
1 92913536 intron variant G/A snv 0.35 2
rs7872515
SPTLC1
0.925 0.040 9 92060258 intron variant G/A snv 0.25 4
rs669
A2M ; KLRG1
0.851 0.080 12 9079672 missense variant T/C snv 0.31 0.33 7
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs12527359 6 89018502 intergenic variant T/A snv 0.23 2
rs4916723
LINC00461
0.925 0.040 5 88558577 intron variant A/C;G;T snv 4
rs2023239
CNR1
0.724 0.160 6 88150763 intron variant T/C snv 0.21 20
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs59190448
OXTR ; CAV3
3 8761315 intron variant G/A snv 0.12 1
rs2254298
CAV3 ; OXTR
0.701 0.200 3 8760542 intron variant G/A snv 0.16 23
rs1806864 9 87416754 regulatory region variant G/C snv 7.4E-02 2
rs13438494
PCLO
1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs6296
HTR1B ; LOC105377864
0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs3811939
CRHBP
1.000 0.080 5 76954762 intron variant G/A snv 0.27 2
rs3771829
TACR1
0.790 0.120 2 75137019 intron variant C/G snv 0.11 9
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23