Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs524772 3 150729892 downstream gene variant G/A snv 0.98 2
rs3108962
NFRKB
11 129895558 5 prime UTR variant A/G snv 0.98 2
rs34651
TNPO1
1.000 0.040 5 72848178 non coding transcript exon variant C/T snv 0.94 5
rs11133613
SLC12A7
5 1074936 intron variant A/G snv 0.91 2
rs7252007
AP1M2
19 10577081 intron variant T/C snv 0.90 2
rs9438901
RSRP1
1 25258485 intron variant G/A snv 0.89 2
rs1548770 14 74219855 intergenic variant C/T snv 0.88 2
rs2370823
LINC02381 ; SMUG1
12 54138553 intron variant G/A snv 0.88 2
rs2955088
EEFSEC
3 128244867 intron variant C/T snv 0.86 4
rs634454
LOC105376214
9 108150874 regulatory region variant T/G snv 0.86 2
rs2275707
SLC30A10
1 219914705 3 prime UTR variant C/A snv 0.85 2
rs778986
FUT3
1.000 0.080 19 5844526 missense variant A/G snv 0.84 0.84 2
rs4951378
ATP2B4
1 203689654 intron variant A/G snv 0.83 4
rs6792151
PLD1
3 171812145 upstream gene variant T/G snv 0.83 2
rs1419114
ATP2B4
1 203683316 synonymous variant A/G snv 0.88 0.83 3
rs10900586
ATP2B4
1 203684957 intron variant G/A snv 0.83 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs10883353 10 99496351 intergenic variant G/A snv 0.82 2
rs380267 19 54295230 upstream gene variant G/A snv 0.82 3
rs35995659
LINC00216 ; PSMA3-AS1 ; ARMH4
14 58287055 intron variant -/TT ins 0.82 2
rs4703877 5 72430085 intergenic variant G/A snv 0.81 2
rs2016409
ATOX1
5 151746763 intron variant G/T snv 0.81 2
rs1029555 7 26547477 upstream gene variant T/C snv 0.80 2
rs12449852
CDK12
1.000 0.080 17 39475835 intron variant A/G snv 0.79 3
rs1042034
APOB
0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 9