Source: GWASCAT ×
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 2
rs10045497
HMGCR
5 75340659 intron variant C/A snv 0.35 2
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10066168
HAVCR1
5 157057207 intron variant C/G;T snv 2
rs10102164
RP1
8 54509054 upstream gene variant G/A snv 0.19 3
rs10104003
RP1
8 54509880 intron variant C/T snv 0.19 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
rs1016988 5 132408882 upstream gene variant T/C snv 0.20 2
rs10172650 2 20982585 intergenic variant G/A snv 0.28 2
rs10176901
ABCB11
2 168974151 intron variant G/A snv 0.57 2
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs10199768
APOB
2 21021128 intron variant G/T snv 0.35 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
rs10275712
GPR146 ; C7orf50
7 1043282 intron variant G/A snv 0.18 1
rs1030431 8 58399138 intergenic variant A/G;T snv 3
rs1038026
TOMM40
1.000 0.080 19 44901805 3 prime UTR variant A/G;T snv 3
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 4
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 4
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 6
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs10460181
LOC107985305 ; IGSF23
19 44636865 intron variant A/G;T snv 0.26 2