Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs652438
MMP12
0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 14
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs10903323
MSRA
0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs12411886
CNNM2
0.882 0.080 10 102925542 intron variant C/A snv 7.8E-02 3
rs640198
MMP13
0.851 0.040 11 102954362 intron variant T/G snv 0.68 4
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 9
rs11191548
CNNM2
0.882 0.080 10 103086421 3 prime UTR variant T/C snv 8.6E-02 10
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 6
rs1165668
TTC41P
1.000 0.040 12 103924218 intron variant G/A snv 0.71 1
rs1165669
TTC41P
1.000 0.040 12 103924394 intron variant A/G snv 0.71 1
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 3
rs1042620356
GSTO1
1.000 0.040 10 104259596 missense variant A/G snv 1
rs2385168
LHFPL3
1.000 0.040 7 104438209 intron variant C/A;T snv 0.41 1
rs189889864 0.925 0.040 9 104634643 downstream gene variant G/A snv 2.8E-03 2
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
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
rs2066718
ABCA1
0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 7
rs2515629
ABCA1
1.000 0.040 9 104832083 intron variant A/G snv 0.16 3
rs532997003
ABCA1
0.882 0.040 9 104840464 missense variant T/C snv 2.0E-05 3
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