Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34911341
GHRL ; GHRLOS
0.882 0.200 3 10289835 missense variant C/T snv 7.0E-03 7.3E-03 5
rs26802
GHRLOS ; GHRL
0.925 0.160 3 10290681 intron variant T/G snv 0.31 3
rs26312
GHRL ; GHRLOS
0.925 0.080 3 10291174 5 prime UTR variant G/A snv 0.16 2
rs3759579
MARK3
0.925 0.120 14 103384935 upstream gene variant A/G snv 0.55 2
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1545
MKKS
0.925 0.080 20 10405365 missense variant C/A snv 0.14 0.14 2
rs1547
MKKS
0.925 0.080 20 10405411 missense variant G/A snv 0.14 0.14 2
rs74315394
MKKS
0.851 0.440 20 10412791 missense variant C/A snv 5.2E-03 5.0E-03 4
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs2515602
ABCA1
1.000 0.080 9 104837887 intron variant A/G snv 0.47 1
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs10953454
LHFPL3
1.000 0.080 7 104863366 intron variant G/A snv 0.12 1
rs2275542
ABCA1
1.000 0.080 9 104882799 intron variant C/T snv 0.28 1
rs3890182
ABCA1
0.925 0.120 9 104885374 intron variant G/A;T snv 5
rs1800976
ABCA1 ; LOC105376196
1.000 0.080 9 104928428 intron variant C/G snv 0.47 2
rs2272495
APPL2
1.000 0.080 12 105190099 missense variant G/A snv 0.21 0.18 1
rs1107756
APPL2 ; C12orf75
1.000 0.080 12 105235461 intron variant A/G snv 0.33 1
rs4730153
NAMPT
0.882 0.120 7 106263704 intron variant A/G snv 0.49 3
rs3801266
NAMPT
0.925 0.080 7 106283804 intron variant T/C snv 0.26 3
rs1319501
NAMPT
0.882 0.120 7 106285307 intron variant C/A;T snv 0.76 4
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs35669975 0.925 0.120 13 107138053 intergenic variant C/A;G snv 2
rs1281685502
ATM
1.000 0.080 11 108292629 missense variant A/G;T snv 4.0E-06; 4.0E-06 1