Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs632793 0.882 0.120 1 11850620 upstream gene variant A/G snv 0.45 3
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs717620
ABCC2
0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs4994
ADRB3
0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs974389711
APOA1 ; APOA1-AS
1.000 0.040 11 116836210 synonymous variant C/T snv 1
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs676210
APOB
0.925 0.120 2 21008652 missense variant G/A;T snv 0.29 12
rs679899
APOB
0.925 0.080 2 21028042 missense variant G/A snv 0.49 0.39 7
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs11542041
APOE
0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs267606661
APOE
0.763 0.120 19 44909101 missense variant C/G;T snv 3.9E-04; 1.0E-05 10
rs573658040
APOE
0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 9
rs764929617
APOE
0.776 0.200 19 44907799 missense variant C/T snv 4.0E-06 8
rs769455
APOE
0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 8
rs140808909
APOE
0.851 0.120 19 44909080 missense variant G/A snv 2.0E-04 5.6E-05 5
rs121918392
APOE
0.925 0.040 19 44907777 missense variant G/A snv 3.6E-05 7.0E-06 2
rs1444332461
ARSA
1.000 0.040 22 50627185 missense variant A/G snv 4.1E-06 1
rs10748835
AS3MT ; LOC107984265 ; BORCS7-ASMT
0.827 0.160 10 102900499 non coding transcript exon variant G/A snv 0.41 5
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 12