Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1023890 1.000 0.080 4 117780291 intergenic variant G/A;C snv 1
rs11072508 1.000 0.080 15 74770056 regulatory region variant C/T snv 0.43 1
rs11986063 1.000 0.080 8 116628076 regulatory region variant C/T snv 0.12 1
rs1583661 1.000 0.080 4 93941116 intergenic variant C/A;T snv 1
rs1870481 1.000 0.080 4 117741865 intergenic variant C/T snv 0.55 1
rs2128383 1.000 0.080 8 129808389 intergenic variant A/G snv 0.15 1
rs2169059 1.000 0.080 4 117786035 intergenic variant C/A snv 0.56 1
rs2170568 1.000 0.080 8 129808129 intergenic variant T/A snv 0.15 1
rs2209907 1.000 0.080 9 80554440 regulatory region variant A/G snv 0.13 1
rs367615 1.000 0.080 5 109613236 intergenic variant C/G;T snv 1
rs4140904 1.000 0.080 4 18314369 intergenic variant A/G snv 0.32 1
rs4460629 0.882 0.080 1 155162859 intergenic variant T/C snv 0.56 1
rs4574118 1.000 0.080 2 106331987 intergenic variant C/G snv 0.84 1
rs7006896 1.000 0.080 8 129809948 regulatory region variant G/A snv 0.13 1
rs7553007 0.827 0.120 1 159728759 intergenic variant G/A snv 0.31 1
rs7667693 1.000 0.080 4 93944123 intergenic variant T/C snv 0.35 1
rs7988900 1.000 0.080 13 97826281 intergenic variant T/C snv 0.45 1
rs879872 1.000 0.080 11 256714 downstream gene variant C/T snv 4.1E-02 1
rs189206655
ABCA1
1.000 0.080 9 104809521 missense variant C/T snv 4.0E-06 1.4E-05 1
rs2231137
ABCG2
0.752 0.400 4 88139962 missense variant C/T snv 0.11 7.4E-02 1
rs1357271377
ACACA
1.000 0.080 17 37161959 missense variant C/T snv 1.6E-05 1
rs754740225
ACAP1
1.000 0.080 17 7343420 missense variant G/A;T snv 3.6E-05; 4.0E-06 1
rs754494408
ACIN1
1.000 0.080 14 23061417 missense variant C/A;T snv 4.0E-06; 2.0E-05 1
rs753267653
ACSL4
1.000 0.080 X 109682851 missense variant G/A snv 2.7E-05 9.5E-06 1
rs782721280
ACTL9
1.000 0.080 19 8697708 missense variant C/T snv 1.6E-05 1