Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs545971
ABO
9 133267960 intron variant T/A;C snv 8
rs643434
ABO
9 133266942 intron variant A/G;T snv 8
rs674302
ABO
9 133271249 intron variant A/T snv 8
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 7
rs644234
ABO
9 133266804 intron variant G/T snv 7
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 6
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 6
rs6065906 20 45925376 downstream gene variant T/A;C;G snv 6
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs1077834
LIPC ; ALDH1A2
15 58431280 intron variant T/C snv 0.34 5
rs10832027
ARNTL
11 13335636 intron variant G/A snv 0.67 5
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 5
rs10512597
RAB37 ; CD300LF
17 74703694 intron variant T/A;C snv 4
rs1490384 6 126530014 intron variant C/G;T snv 4
rs3758348
SURF4
9 133372523 intron variant G/C snv 0.13 4
rs4465830
ZNF335
20 45956781 intron variant A/G snv 0.13 4
rs7518199
IL6R
1 154434943 intron variant A/C;T snv 0.39; 4.2E-06 4
rs10485165
LOC105377885
6 88403098 intron variant C/G;T snv 3
rs11220463
ST3GAL4
11 126378316 intron variant A/T snv 0.12 3