Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7555693 0.925 0.040 1 106295917 intergenic variant G/A snv 0.45 3
rs75995702 0.925 0.040 11 42785177 intergenic variant C/G;T snv 3
rs77826363 0.882 0.040 6 1128802 intergenic variant G/T snv 2.2E-02 3
rs78087832 0.925 0.040 2 224600060 intergenic variant C/T snv 2.4E-03 3
rs7828021 0.925 0.040 8 49727454 intergenic variant C/G;T snv 3
rs9364726 0.882 0.040 6 164236705 intergenic variant A/G snv 6.5E-02 3
rs10233018 0.925 0.040 7 117883655 non coding transcript exon variant A/G snv 0.53 2
rs10485715 0.925 0.040 20 7279278 intergenic variant T/C snv 5.5E-02 2
rs10809520 0.925 0.040 9 11557797 intergenic variant C/T snv 0.28 2
rs195478 0.925 0.040 6 115851928 intergenic variant C/A;G snv 2
rs4685959 0.925 0.040 3 5645577 regulatory region variant C/G;T snv 2
rs4810896 0.925 0.040 20 48918761 upstream gene variant A/C;G snv 2
rs75921243 0.925 0.040 8 9988356 intron variant T/G snv 1.9E-02 2
rs76767803 0.925 0.040 3 36230378 intergenic variant C/T snv 0.16 2
rs3760138
AANAT
0.807 0.160 17 76467027 intron variant G/A;T snv 6
rs4238989
AANAT
0.851 0.120 17 76467306 intron variant C/G snv 0.45 4
rs8150
AANAT ; RHBDF2
0.807 0.160 17 76470935 3 prime UTR variant G/A;C snv 6
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs1415088003
ACE
0.827 0.160 17 63489038 synonymous variant C/T snv 4.0E-06 7
rs16875288
ADAMTS16 ; LOC101929200
0.851 0.040 5 5297087 intron variant A/T snv 0.22 4
rs143405544
ADAMTS6
0.925 0.040 5 65459777 intron variant A/G snv 4.8E-03 3
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12