Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2811709
CDKN2A
1.000 0.120 9 21980152 intron variant A/G snv 0.88 1
rs3731201
CDKN2A
1.000 0.080 9 21988897 intron variant C/T snv 0.86 2
rs7036656
CDKN2A
9 21990458 intron variant C/T snv 0.74 1
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs2811710
CDKN2A
1.000 0.160 9 21991924 intron variant C/T snv 0.47 1
rs2518720
CDKN2A
0.925 0.080 9 21978980 intron variant C/T snv 0.43 2
rs3731239
CDKN2A
0.763 0.240 9 21974219 intron variant A/G snv 0.26 10
rs61271866
CDKN2B-AS1 ; CDKN2A
1.000 0.080 9 21997016 intron variant T/A snv 0.19 1
rs3088440
CDKN2A ; CDKN2A-DT
0.776 0.240 9 21968160 3 prime UTR variant G/A snv 0.13 12
rs4074785
CDKN2A
1.000 0.080 9 21981584 intron variant G/A snv 0.12 1
rs3731246
CDKN2A
0.882 0.120 9 21971990 intron variant C/G snv 0.11 3
rs3731245
CDKN2A
0.925 0.120 9 21972446 intron variant C/T snv 6.6E-03 2
rs116150891
CDKN2A
1.000 0.040 9 21970929 missense variant G/A;C snv 5.6E-04 2.6E-03 1
rs3731199
CDKN2A
9 21989331 intron variant T/C snv 2.4E-03 2
rs45456595
CDKN2A
9 21974641 missense variant C/G snv 2.0E-03 2.1E-03 1
rs3731236
CDKN2A
9 21976977 intron variant G/A snv 1.9E-03 2
rs3731215
CDKN2A
9 21985772 intron variant A/G snv 1.2E-03 5
rs200863613
CDKN2A
0.925 0.080 9 21971061 missense variant C/A;T snv 8.5E-05 3.7E-04 6
rs372670098
CDKN2A
9 21971153 missense variant T/C snv 9.5E-06 2.8E-05 1
rs779306249
CDKN2A ; CDKN2B-AS1
1.000 0.120 9 21994234 frameshift variant -/C delins 1.7E-05 1.4E-05 1
rs770859592
CDKN2A
1.000 0.080 9 21974599 missense variant C/T snv 1.6E-05 1.4E-05 1
rs1060501266
CDKN2A
1.000 0.120 9 21968347 intron variant T/C snv 7.0E-06 1
rs1390902532
CDKN2A
1.000 0.040 9 21968766 missense variant T/C snv 7.4E-06 7.0E-06 2
rs773459232
CDKN2A ; CDKN2B-AS1
1.000 0.080 9 21994286 missense variant C/T snv 7.0E-06 1
rs749714198
CDKN2A
0.882 0.200 9 21971100 missense variant G/A snv 8.6E-06 7.0E-06 4