Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1038026
TOMM40
1.000 0.080 19 44901805 3 prime UTR variant A/G;T snv 4
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 7
rs10402729
NCAN
19 19244291 intron variant T/C snv 3.3E-02 4
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs10415849
GATAD2A
19 19394278 intron variant C/T snv 0.12 4
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 6
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 11
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 15
rs10433493
IL1RAP
3 190647811 intron variant G/C snv 1.8E-02 2
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10460181
LOC107985305 ; IGSF23
19 44636865 intron variant A/G;T snv 0.26 2
rs10474434
HMGCR
5 75348856 intron variant G/T snv 0.20 3
rs1047743
UNK
17 75794012 3 prime UTR variant C/G;T snv 1
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs10484766
ARG1 ; MED23
6 131578846 intron variant C/T snv 3.3E-02 4
rs10490120 2 48916690 intron variant A/G snv 9.3E-02 1
rs10490626
LOC107985940
2 118078265 intergenic variant G/A snv 5.2E-02 3
rs10495399
RYR2
1 237648783 intron variant T/G snv 5.5E-02 2
rs10500212
PBX4
19 19612406 intron variant C/T snv 0.10 4
rs10504062
PRKDC
8 47824663 intron variant T/C snv 2.1E-02 3
rs10513551
TRIM59-IFT80 ; IFT80
3 160368267 intron variant G/T snv 0.53 1
rs10518982
LIPC
15 58507555 intron variant A/G snv 2.2E-02 3
rs1065853 19 44909976 non coding transcript exon variant G/A;C;T snv 5
rs10744775
BRAP
12 111658411 intron variant T/C snv 0.44 2