Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs548145 2 21068440 regulatory region variant T/C snv 0.68 1
rs553427 1 234717013 intron variant C/T snv 0.65 1
rs56167574 7 151548889 intergenic variant G/A snv 5.4E-02 1
rs577584 2 21076995 intergenic variant T/A snv 0.68 1
rs58198139 5 156972028 intergenic variant C/G;T snv 1
rs6016381 20 40551796 regulatory region variant T/C snv 0.40 1
rs66883945 6 138996690 regulatory region variant -/C;CC delins 1
rs72834327 2 117842293 downstream gene variant A/T snv 5.7E-02 1
rs73219351 2 17295273 intergenic variant T/C;G snv 1
rs75214121 8 58485717 downstream gene variant C/T snv 2.5E-02 1
rs7523141 1 55033125 intergenic variant C/A;T snv 1
rs7538216 1 16183176 intergenic variant T/A;C snv 1
rs77645768 4 72803111 upstream gene variant G/A snv 1.8E-02 1
rs79316815 1 2902742 intergenic variant A/G snv 9.2E-02 1
rs79588679 18 22327807 intergenic variant C/T snv 0.11 1
rs79950627 11 2212560 intergenic variant G/A snv 2.1E-02 1
rs7873387
ABCA1
9 104833321 intron variant A/C snv 0.20 1
rs2389606
ABCB11
2 168973262 intron variant C/T snv 0.57 1
rs112959129
ABHD11-AS1
7 73733661 upstream gene variant -/CA delins 1
rs56903760
ALDH1A2
15 58400482 intron variant C/T snv 5.5E-02 1
rs72653060
APOB
2 21034825 missense variant A/C snv 9.9E-05 5.0E-04 1
rs535064984
ASGR2
17 7116978 upstream gene variant T/C snv 3.7E-03 1
rs118147862
BCAM
19 44816374 intron variant G/A snv 2.4E-02 1
rs11638450
CEMIP ; LOC107984749
15 80898191 intron variant C/T snv 0.33 1
rs17029617
CMTM6
3 32500061 intron variant G/A snv 0.14 1