Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs174533
MYRF ; TMEM258
0.763 0.160 11 61781553 intron variant G/A snv 0.37 0.29 18
rs9929218
CDH1
0.732 0.160 16 68787043 intron variant G/A snv 0.28 16
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 14
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs7229639
SMAD7
0.763 0.080 18 48924606 intron variant A/G snv 0.87 13
rs4759277
LRP1
0.752 0.160 12 57139907 intron variant C/A snv 0.38 12
rs6058093
PIGU
0.776 0.080 20 34625392 intron variant A/C snv 0.55 12
rs11874392
SMAD7
0.763 0.080 18 48926786 intron variant A/T snv 0.50 11
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 11
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 11
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85 11
rs35107139
BMP4
0.776 0.080 14 53952388 intron variant A/C;G;T snv 11
rs10049390
SLCO2A1
0.776 0.080 3 133982275 intron variant G/A snv 0.67 10
rs10980628
LPAR1
0.776 0.080 9 110909123 intron variant T/C snv 0.16 10
rs11196170
TCF7L2
0.776 0.080 10 112962862 intron variant G/A;C snv 10
rs117079142
LOC112268030 ; UTP23
0.776 0.080 8 116778675 intron variant C/A snv 3.0E-02 10
rs11884596
LOC105373831
0.776 0.080 2 198747683 intron variant T/C snv 0.32 10
rs12246635
VTI1A
0.776 0.080 10 112528860 intron variant T/C snv 0.13 10
rs12372718
ATF1
0.776 0.080 12 50777307 intron variant A/G snv 0.35 10
rs1250567
ZMIZ1
0.776 0.080 10 79286508 intron variant T/C snv 0.56 10