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
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs2954031 8 125479491 intron variant G/T snv 0.42 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs9942416 5 75741470 intergenic variant C/G snv 0.53 9
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 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
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34 7
rs1801689
APOH
17 66214462 missense variant A/C;G snv 4.0E-06; 2.4E-02; 4.8E-05 7
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs3747207
PNPLA3
22 43928975 intron variant G/A snv 0.22 7
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 7
rs7499892
CETP
16 56972678 intron variant C/G;T snv 7
rs9376090
HBS1L
6 135090090 intron variant T/C snv 0.19 7
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 6
rs11207997
DOCK7 ; ANGPTL3
1 62596235 intron variant C/T snv 0.39 6