Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174577
FADS2
1.000 0.080 11 61837342 intron variant C/A snv 0.38 12
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 8
rs56113850
CYP2A6
0.807 0.080 19 40847202 intron variant T/C snv 0.52 8
rs1062980
IREB2
0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 6
rs259919
ZNRD1ASP
0.882 0.080 6 30057726 intron variant G/A snv 0.25 6
rs3813565
LOC105370913 ; CHRNB4
0.851 0.080 15 78727268 splice region variant G/A;T snv 6
rs10519203
HYKK
0.851 0.080 15 78521704 intron variant G/A snv 0.67 5
rs11638372
LOC112268142 ; CHRNB4
0.925 0.080 15 78691217 intron variant C/A;G;T snv 0.28 5
rs2036534
HYKK
0.827 0.080 15 78534606 3 prime UTR variant T/C snv 0.26 5
rs6495309
CHRNB4 ; CHRNA3
0.807 0.080 15 78622903 upstream gene variant C/A;T snv 5
rs938682
CHRNA3
0.851 0.080 15 78604205 intron variant G/A snv 0.72 5
rs12910984
CHRNA3
0.827 0.080 15 78599285 intron variant G/A;C;T snv 4
rs1394371 0.925 0.080 15 78432127 intergenic variant C/T snv 0.22 4
rs1489759
LOC105377462
0.882 0.080 4 144553321 intron variant A/G snv 0.43 4
rs1996371
LOC112268142 ; CHRNB4
1.000 0.080 15 78664464 intron variant T/C snv 0.28 4
rs2656069
IREB2
0.882 0.080 15 78453365 intron variant C/G;T snv 4
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 4
rs4887077
CHRNB4 ; LOC112268142
1.000 0.080 15 78686022 intron variant C/T snv 0.28 4
rs6495314
CHRNB4 ; LOC112268142
0.925 0.080 15 78668187 intron variant A/C snv 0.35 4
rs931794
HYKK
0.851 0.080 15 78533838 3 prime UTR variant G/A;C snv 4
rs11637630
CHRNA3
0.882 0.080 15 78607377 intron variant G/A snv 0.71 3
rs12441998
CHRNB4
0.925 0.080 15 78637030 intron variant G/A snv 0.63 3
rs12594247
CHRNB4
0.925 0.080 15 78654291 intron variant C/T snv 0.14 3
rs1316971
CHRNB4
0.925 0.080 15 78638168 intron variant A/G;T snv 0.62 3
rs174534
MYRF ; TMEM258
1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28 3