Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs876538 1 159705927 upstream gene variant T/A;C snv 2
rs943580 1 230701298 upstream gene variant G/A snv 0.42 2
rs1149643 1 56163763 intron variant A/T snv 0.49 1
rs12731208
PHF13
1 6616425 intron variant T/A;C;G snv 1
rs12758407
HNRNPFP1
1 42041342 non coding transcript exon variant T/A;G snv 1
rs145886902
PCSK9
1 55040006 stop gained G/A;T snv 1.9E-04 1
rs16835282
LINC01031
1 193326609 intron variant T/C snv 0.30 1
rs1800805
SELP
1 169632043 upstream gene variant C/T snv 0.31 1
rs2205849
C1orf112 ; SELL
1 169712216 intron variant T/C snv 0.19 1
rs2820290
IPO9-AS1 ; NAV1
1 201814554 intron variant A/G snv 0.45 1
rs28711771 1 16093094 intergenic variant G/A snv 0.52 1
rs3176867
VCAM1
1 100728649 intron variant C/A;T snv 1
rs448385 1 25068642 intron variant G/A snv 0.41 1
rs56153133
CLCN6
1 11825590 intron variant A/G snv 0.14 1
rs59980837
NGF-AS1
1 115284645 intron variant G/T snv 3.7E-02 1
rs61772626
PLPP3
1 56549996 intron variant A/G snv 0.11 1
rs6670508
RERE
1 8587858 intron variant G/A;C snv 0.62 1
rs6679817 1 88897581 intergenic variant C/T snv 0.25 1
rs6683021 1 232394844 downstream gene variant A/G snv 0.30 1
rs693482
JAK1
1 64897943 intron variant A/C snv 1
rs763781510
DOCK7 ; ANGPTL3
1 62597738 missense variant A/G snv 4.0E-06 1
rs867515118
ESPN ; TNFRSF25
1 6461643 missense variant C/T snv 1
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29