Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3131379
MSH5 ; MSH5-SAPCD1
0.752 0.440 6 31753256 intron variant G/A snv 6.4E-02 7.9E-02 6
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 6
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 6
rs380286
CLPTM1L
0.776 0.200 5 1320132 intron variant G/A snv 0.47 6
rs558702
C2 ; ZBTB12 ; CYP21A2
0.807 0.320 6 31902549 intron variant G/A snv 7.7E-02 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
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 5
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs3129791
HCG15
0.827 0.280 6 28986516 intron variant G/A snv 5.3E-02 5
rs31489
CLPTM1L
0.763 0.320 5 1342599 intron variant C/A snv 0.41 5
rs3817963
TSBP1-AS1 ; BTNL2
0.776 0.360 6 32400310 intron variant T/C snv 0.25 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
rs13211507
PGBD1
0.882 0.200 6 28289600 intron variant T/C snv 6.4E-02 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
rs3117143
LOC100129636
0.882 0.160 6 29063365 intron variant C/A snv 5.2E-02 4
rs4380028
MORF4L1
0.807 0.120 15 78818751 intron variant C/T snv 0.34 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
rs667282
CHRNA5
0.790 0.120 15 78571130 intron variant T/C snv 0.28 4
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 4
rs11637630
CHRNA3
0.882 0.080 15 78607377 intron variant G/A snv 0.71 3