Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10038095
HMGCR
5 75341886 intron variant A/T snv 0.38 3
rs10045497
HMGCR
5 75340659 intron variant C/A snv 0.35 1
rs10047462
APOA1-AS ; SIK3
11 116851325 intron variant G/C;T snv 2
rs10102164
RP1
8 54509054 upstream gene variant G/A snv 0.19 3
rs10115928
ABCA1
9 104888562 intron variant C/T snv 0.47 1
rs10128711
SPTY2D1
11 18611437 intron variant T/C snv 0.64 0.55 1
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs10199768
APOB
2 21021128 intron variant G/T snv 0.35 5
rs10220503
NPC2 ; MIR4709
14 74480389 3 prime UTR variant C/A snv 1.1E-02 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs10260606 7 44544952 upstream gene variant G/A;C snv 2
rs1029040
PCSK5
9 76038907 intron variant T/C snv 8.3E-02 1
rs10306137
PTGS1
9 122376185 intron variant C/T snv 1.8E-02 3
rs1038026
TOMM40
1.000 0.080 19 44901805 3 prime UTR variant A/G;T snv 1
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 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 4
rs1042031
APOB
0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 3
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 10
rs10474434
HMGCR
5 75348856 intron variant G/T snv 0.20 3
rs10478730
EDN1
6 12297276 downstream gene variant C/T snv 1.2E-02 5
rs10490626
LOC107985940
2 118078265 intergenic variant G/A snv 5.2E-02 3