Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11383346
LOC107984462 ; LOC105369710
12 28130254 upstream gene variant -/T delins 0.58 2
rs139887111
TET2 ; TET2-AS1
4 105195057 intron variant -/T delins 0.31 1
rs199640474
EYS
6 64295335 intron variant A/- delins 1
rs201609026 4 32979435 intergenic variant A/-;AA;AAA delins 1
rs34480284 4 105143470 upstream gene variant A/-;AA;AAA delins 1
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 9
rs3995090
LOC107986462 ; HTR4
1.000 0.040 5 148466252 intron variant A/C snv 0.39 5
rs2277027
ADAM19
5 157505368 intron variant A/C snv 0.42 4
rs973796
LOC105377462
4 144502816 intron variant A/C snv 0.31 4
rs1102077 6 139950220 intron variant A/C snv 0.21 3
rs11852372
HYKK
1.000 0.040 15 78509052 intron variant A/C snv 0.27 3
rs2656052
IREB2
15 78448590 intron variant A/C snv 0.36 3
rs11709725
RUVBL1
3 128139090 intron variant A/C snv 0.14 2
rs11858992
CFDP1
16 75377547 intron variant A/C snv 0.52 2
rs13107186
LOC105377462
4 144522887 intron variant A/C snv 0.63 2
rs13329271
CHRNA3
15 78621888 upstream gene variant A/C snv 0.27 2
rs1542726 4 144594617 intron variant A/C snv 0.68 2
rs1595029
RSRC1
3 158523978 intron variant A/C snv 0.52 2
rs17009288 1 221030957 regulatory region variant A/C snv 0.30 2
rs181020201
C1orf185
1.000 0.040 1 51134390 intron variant A/C snv 1.1E-04 2
rs2202572
LINC01416
18 55899240 intron variant A/C snv 0.66 2
rs2811536
EEFSEC
3 128270076 intron variant A/C snv 0.86 2
rs2955081
EEFSEC
3 128241456 intron variant A/C snv 0.86 2
rs35440220
LOC105377462
4 144478680 intron variant A/C snv 0.32 2
rs35937742
LOC105377462
4 144504697 intron variant A/C snv 0.33 2