Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34642455
CYP3A4
7 99777087 intron variant T/C snv 8.8E-03 1
rs7078003
HOGA1
10 97599655 non coding transcript exon variant C/T snv 0.14 0.14 3
rs2072510
LTA4H ; LOC102723340
12 96009421 non coding transcript exon variant G/A snv 0.49 2
rs7954638
CCDC38
12 95921017 intron variant C/A snv 0.53 2
rs72751339
MCTP2
15 94422181 intron variant C/T snv 4.0E-02 1
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs112635299
SERPINA2
1.000 0.040 14 94371805 downstream gene variant G/T snv 1.3E-02 7
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87 6
rs10466351 11 92964815 upstream gene variant C/T snv 0.48 3
rs28645201
CCSER1
4 90607776 intron variant A/G snv 3.7E-02 2
rs75603564
LOC105370615
14 89038109 intergenic variant C/T snv 3.4E-02 2
rs9637599
PPM1K ; PPM1K-DT
4 88285078 intron variant A/C snv 0.56 3
rs34226052 4 88242371 intergenic variant A/G snv 0.22 2
rs10083777
LOC107984858 ; CENPN
16 81031677 intron variant C/T snv 0.15 2
rs1986734
SHROOM3
1.000 0.120 4 76499631 intron variant C/T snv 0.43 3
rs3921
CXCL10 ; ART3
0.807 0.240 4 76021790 3 prime UTR variant C/G snv 0.61 8
rs73359750
RHBDD2
7 75848924 intron variant C/T snv 0.14 1
rs184650103 4 73984932 upstream gene variant C/G;T snv 2
rs16850073
CXCL6
4 73838282 3 prime UTR variant C/T snv 0.29 5
rs2287997
DHX38
16 72106654 intron variant G/A snv 0.17 2
rs77303550
TXNL4B
16 72045758 intron variant C/T snv 0.19 6
rs74249229 16 69945368 downstream gene variant C/T snv 4.2E-02 2
rs172642
C17orf100 ; SLC13A5 ; ALOX15P1
17 6692079 intron variant A/C snv 0.64 2
rs181929163
CEP112
17 65744427 intron variant T/C snv 4.4E-03 1
rs10211524
LOC107984063 ; LINC02245
2 64980940 intron variant G/A snv 0.51 4