Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10019888 4 26061368 regulatory region variant A/G snv 0.17 2
rs10054063 5 173965395 downstream gene variant A/T snv 0.26 4
rs10087900 8 143221248 downstream gene variant G/A snv 0.37 1
rs10091038 8 29502788 intergenic variant A/C snv 0.57 1
rs1009360
LOC107984063 ; LINC02245 ; LINC02576
2 65048915 intron variant T/C snv 0.51 2
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 2
rs10105606 8 19970337 downstream gene variant C/A snv 0.42 2
rs10106652 1.000 0.040 8 20070649 intergenic variant G/A snv 0.29 3
rs1011731
DNM3 ; PIGC
1 172377408 intron variant G/A snv 0.46 4
rs10127775
GALNT2
1 230160042 intron variant A/G;T snv 4
rs10184004 1.000 0.080 2 164651879 downstream gene variant C/T snv 0.48 5
rs10185855
TBC1D8
2 101025798 intron variant A/G snv 0.35 4
rs10198423 2 85333439 upstream gene variant G/A;C;T snv 1
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs1026422 7 50280211 upstream gene variant G/A snv 0.51 1
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 3
rs1037116 15 101528701 upstream gene variant C/T snv 0.20 2
rs1037378
PDE3B
11 14830944 intron variant G/A snv 0.52 1
rs1038026
TOMM40
1.000 0.080 19 44901805 3 prime UTR variant A/G;T snv 3
rs10401176
BCL3
1.000 0.080 19 44750234 intron variant C/G;T snv 0.17 2
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