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
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs2954031 8 125479491 intron variant G/T snv 0.42 9
rs4665972
SNX17
2 27375230 intron variant T/C snv 0.69 9
rs630014
ABO
9 133274306 intron variant G/A;C snv 9
rs12721046
APOC1
19 44917997 intron variant G/A snv 0.11 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
rs11902417 2 20976028 intergenic variant G/A snv 0.25 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 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
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs8177318
INHCAP ; TF
3 133748533 missense variant T/A snv 1.6E-04 2.9E-04 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
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs11568746
TGFBR1
9 99105926 intron variant C/G snv 2.1E-05 6