Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1489759
LOC105377462
0.882 0.080 4 144553321 intron variant A/G snv 0.43 7
rs11637630
CHRNA3
0.882 0.080 15 78607377 intron variant G/A snv 0.71 6
rs7177514
CHRNA3
0.882 0.080 15 78615064 intron variant C/G;T snv 6
rs78768932
PXN
0.882 0.080 12 120222977 missense variant C/G;T snv 5.4E-03 5.4E-03 6
rs8042059
CHRNA3
0.882 0.080 15 78615517 intron variant A/C;T snv 6
rs1019340046
TP53
0.882 0.080 17 7674225 missense variant C/T snv 5
rs1329032366
PDLIM5
0.882 0.080 4 94654530 missense variant A/G snv 4.0E-06 5
rs1330189219
LTA ; LOC100287329 ; TNF
0.882 0.080 6 31573570 synonymous variant C/T snv 4.0E-06 5
rs35755165 0.882 0.080 19 40840084 intron variant A/C;G snv 5
rs374733251
MET
0.882 0.080 7 116740993 missense variant A/G snv 6.0E-05 7.7E-05 5
rs377444977
EGFR
0.882 0.080 7 55143443 missense variant G/A snv 5.2E-05 2.1E-05 5
rs3842
ABCB1
0.882 0.080 7 87504050 3 prime UTR variant T/C snv 0.16 5
rs5742933
ORMDL1 ; PMS1
0.882 0.080 2 189784590 5 prime UTR variant G/A;C snv 5
rs5744724
POLK
0.882 0.080 5 75599649 3 prime UTR variant G/C snv 5.4E-02 5
rs775514340
CILK1
0.882 0.080 6 53041202 missense variant T/A;C snv 4.0E-06 5
rs1057519857
ERBB2 ; MIR4728
0.882 0.080 17 39724772 missense variant T/C snv 4
rs11072768
CHRNB4
0.882 0.080 15 78637136 intron variant T/C;G snv 4
rs112290073
TERT
0.882 0.080 5 1285917 intron variant G/A snv 7.8E-03 4
rs1169300
HNF1A
0.882 0.080 12 120993422 intron variant G/A snv 0.27 4
rs1192694481
MMP13
0.882 0.080 11 102955629 missense variant C/T snv 4.0E-06 4
rs12072037
MFSD2A
0.882 0.080 1 39954534 upstream gene variant C/A snv 6.1E-02 4
rs1238968510
MMP2
0.882 0.080 16 55479556 missense variant A/G;T snv 4.1E-06 2.1E-05 4
rs125555
MBD1
0.882 0.080 18 50273809 missense variant G/A;C snv 3.6E-05; 0.19 4
rs12740674
GNG12-AS1 ; WLS
0.882 0.080 1 68121775 intron variant C/T snv 0.34 4
rs1347093
LOC105374690 ; MIR217HG
0.882 0.080 2 56019205 intron variant G/T snv 0.21 4