Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11790959 1.000 0.080 9 134127023 intergenic variant C/A;T snv 3.4E-03 1
rs17028719 1.000 0.080 1 5734948 intergenic variant A/G snv 4.8E-02 1
rs17616845 1.000 0.080 7 12741918 intron variant T/C snv 0.15 1
rs1912461 1.000 0.080 15 36052338 intron variant T/C snv 3.3E-02 1
rs1943418 1.000 0.080 18 59812296 intergenic variant T/C snv 0.76 1
rs1995364 1.000 0.080 5 10903669 intergenic variant A/G snv 0.62 1
rs4384980 1.000 0.080 3 182741281 upstream gene variant A/C snv 0.48 1
rs4610908 1.000 0.080 X 35166418 intergenic variant G/A snv 0.24 1
rs567926 1.000 0.080 4 46239752 downstream gene variant G/A snv 0.63 1
rs5916144 1.000 0.080 X 5561570 intergenic variant C/A;G snv 1
rs5961794 1.000 0.080 X 5656287 intron variant A/G snv 0.27 1
rs602618 1.000 0.080 10 111083327 downstream gene variant C/A snv 0.58 1
rs6425323 1.000 0.080 1 175155900 downstream gene variant C/T snv 0.39 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
rs7777391 1.000 0.080 7 117981823 intergenic variant A/G snv 0.60 1
rs9847462 1.000 0.080 3 164840807 intergenic variant A/G snv 0.14 1
rs994029 1.000 0.080 9 86760399 downstream gene variant C/T snv 0.71 1
rs727532
ABLIM1
1.000 0.080 10 114445017 intron variant A/G snv 0.17 1
rs12006002
ADAMTSL1
1.000 0.080 9 18166901 intron variant C/T snv 0.30 1
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs2066702
ADH1B
0.882 0.080 4 99307860 missense variant G/A snv 1.5E-02 5.9E-02 7
rs1789882
ADH1B
1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82 4
rs1789891
ADH1B
1.000 0.080 4 99329262 intron variant C/A snv 0.13 4
rs1154433
ADH1B
1.000 0.080 4 99332551 intron variant A/G;T snv 3