Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 7
rs4380028
MORF4L1
0.807 0.120 15 78818751 intron variant C/T snv 0.34 7
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59 7
rs849140
JAZF1
0.851 0.240 7 28144083 intron variant T/C snv 0.58 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs938682
CHRNA3
0.851 0.080 15 78604205 intron variant G/A snv 0.72 7
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 6
rs11637630
CHRNA3
0.882 0.080 15 78607377 intron variant G/A snv 0.71 6
rs1317286
CHRNA3
0.925 0.120 15 78603787 intron variant A/G snv 0.30 6
rs1812175
HHIP-AS1 ; HHIP
4 144653692 intron variant A/G snv 0.79 6
rs3101336
LOC105378797
1.000 0.080 1 72285502 intron variant T/C snv 0.62 6
rs395962
LIN28B
6 104949543 intron variant T/G snv 0.72 6
rs7173743
MORF4L1
0.851 0.120 15 78849442 intron variant T/C snv 0.45 6
rs7177514
CHRNA3
0.882 0.080 15 78615064 intron variant C/G;T snv 6
rs8042059
CHRNA3
0.882 0.080 15 78615517 intron variant A/C;T snv 6
rs8044769
FTO
0.851 0.200 16 53805223 intron variant T/A;C;G snv 6
rs951266
CHRNA5
0.882 0.080 15 78586199 intron variant G/A snv 0.26 6
rs9788721
HYKK
1.000 0.040 15 78510527 intron variant C/T snv 0.65 6
rs11638372
LOC112268142 ; CHRNB4
0.925 0.080 15 78691217 intron variant C/A;G;T snv 0.28 5
rs11639372
CHRNB4 ; LOC112268142
0.925 0.080 15 78674313 intron variant C/T snv 0.30 5
rs11878604 19 40827379 intron variant T/C snv 0.14 5
rs12902602
LOC112268142 ; CHRNB4
15 78675059 intron variant A/G snv 0.28 5
rs138544659
CHRNA3
1.000 0.040 15 78608359 intron variant T/G snv 0.28 5
rs2047937
ZNF423
0.925 0.120 16 49830880 intron variant C/T snv 0.50 5
rs2371767
ADAMTS9-AS2
3 64732582 intron variant G/C snv 0.38 5