Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9
rs2954031 8 125479491 intron variant G/T snv 0.42 9
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 8
rs12967135 18 60181790 intergenic variant G/A snv 0.24 8
rs4418728 10 93079967 downstream gene variant G/T snv 0.42 8
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs11508026
CETP
16 56965416 intron variant C/T snv 0.32 7
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7
rs11570255
EDN3
1.000 20 59300861 missense variant G/A;T snv 3.3E-03; 2.9E-05 7
rs115849089 8 20054859 intergenic variant G/A snv 9.8E-02 7
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs12679834
LPL
8 19962922 intron variant T/C snv 9.4E-02 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34 7
rs2306363
SIPA1
11 65638129 5 prime UTR variant G/T snv 0.15 7
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7