Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10029254
KLHL8
4 87238988 intron variant C/T snv 0.18 1
rs10038095
HMGCR
5 75341886 intron variant A/T snv 0.38 3
rs10045497
HMGCR
5 75340659 intron variant C/A snv 0.35 2
rs10047462
APOA1-AS ; SIK3
11 116851325 intron variant G/C;T snv 3
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10102164
RP1
8 54509054 upstream gene variant G/A snv 0.19 4
rs1010305
CHD6
20 41472901 intron variant A/G;T snv 0.61 1
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 2
rs1014283
ABCB4
7 87447271 intron variant C/A;T snv 2
rs10156121 7 142672656 downstream gene variant T/C snv 3.9E-02 4
rs10172650 2 20982585 intergenic variant G/A snv 0.28 2
rs10177080
ABCB11
2 168974288 intron variant G/A snv 0.53 1
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 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 18
rs10260606 7 44544952 upstream gene variant G/A;C snv 3
rs1029040
PCSK5
9 76038907 intron variant T/C snv 8.3E-02 1
rs1030431 8 58399138 intergenic variant A/G;T snv 3
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 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
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6