Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs56243511 8 9948185 intergenic variant T/C snv 2
rs9650622 8 9946782 intergenic variant G/T snv 0.40 2
rs483916 8 9936091 intergenic variant A/C snv 0.51 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs55868514 8 9822890 intergenic variant T/C snv 0.57 2
rs1976671 8 9822124 intergenic variant A/C;G;T snv 2
rs73655199
CORO2A
9 98145201 intron variant G/A snv 6.4E-03 1
rs9286060 8 9795635 intergenic variant A/C;T snv 2
rs35231275
TNKS
8 9762399 intron variant T/A snv 0.22 1
rs4383974
TNKS
8 9761838 intron variant C/G snv 0.30 2
rs7902871
SLIT1
10 97049946 intron variant A/G snv 0.21 2
rs12773465
SLIT1
10 97034302 intron variant A/G snv 0.12 2
rs7599598
FER1L5
2 96686103 missense variant A/G;T snv 0.41 2
rs34311866
TMEM175
0.882 0.080 4 958159 missense variant T/C snv 0.18 0.14 6
rs115888294 8 94105161 upstream gene variant T/C snv 2.4E-02 1
rs4847240
DR1
1 93352389 intron variant A/G snv 0.51 3
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs11781008 8 9295729 intron variant G/C;T snv 2
rs10503387 8 9293015 intron variant C/T snv 0.33 2
rs453301 8 9172877 intron variant T/G snv 0.54 3
rs3743832
C16orf72
1.000 0.080 16 9120023 3 prime UTR variant A/C snv 0.55 4
rs4494364 12 91083337 intergenic variant G/A snv 0.17 2
rs991427 12 91080645 intergenic variant C/G;T snv 0.17 2
rs2521501
FES
0.925 0.080 15 90894158 intron variant A/C;T snv 10