Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 2
rs575031539
CDKN2A
0.925 0.080 9 21971020 missense variant C/G;T snv 4.2E-06 2
rs137854599
CDKN2A
0.882 0.080 9 21971093 missense variant C/G;T snv 2
rs759763964
CDKN2A
0.925 0.120 9 21971142 missense variant C/G;T snv 1.4E-05 2
rs878853647
CDKN2A
0.882 0.120 9 21971099 missense variant C/G;T snv 2
rs758389471
CDKN2A
0.882 0.080 9 21971160 missense variant C/G;T snv 4.7E-06; 4.7E-06 2
rs2518723
CDKN2B-AS1 ; CDKN2A
1.000 0.120 9 21995883 non coding transcript exon variant C/G;T snv 1
rs1453633223
CDKN2A
0.807 0.080 9 21974503 missense variant C/T snv 4.0E-06 6
rs1289280947
CDKN2A
0.851 0.080 9 21974571 missense variant C/T snv 4.0E-06 5
rs757066045
CDKN2A
0.882 0.040 9 21974725 missense variant C/T snv 8.2E-06 4
rs2518720
CDKN2A
0.925 0.080 9 21978980 intron variant C/T snv 0.43 2
rs3731245
CDKN2A
0.925 0.120 9 21972446 intron variant C/T snv 6.6E-03 2
rs3731201
CDKN2A
1.000 0.080 9 21988897 intron variant C/T snv 0.86 2
rs1554653960
CDKN2A
0.925 0.040 9 21971007 missense variant C/T snv 1
rs1064794292
CDKN2A
0.882 0.200 9 21974760 missense variant C/T snv 1
rs35741010
CDKN2A
1.000 0.040 9 21971055 missense variant C/T snv 4.3E-06 1
rs1377159790
CDKN2A
9 21971203 start lost C/T snv 4.5E-06 1
rs1309566180
CDKN2A
1.000 0.080 9 21971170 missense variant C/T snv 1
rs773459232
CDKN2A ; CDKN2B-AS1
1.000 0.080 9 21994286 missense variant C/T snv 7.0E-06 1
rs770859592
CDKN2A
1.000 0.080 9 21974599 missense variant C/T snv 1.6E-05 1.4E-05 1
rs3088440
CDKN2A ; CDKN2A-DT
0.776 0.240 9 21968160 3 prime UTR variant G/A snv 0.13 12
rs755927351
CDKN2A
1.000 0.040 9 21970968 missense variant G/A snv 4.1E-06 1
rs4074785
CDKN2A
1.000 0.080 9 21981584 intron variant G/A snv 0.12 1
rs121913387
CDKN2A
0.827 0.160 9 21971187 stop gained G/A;C snv 4.6E-06 4
rs34886500
CDKN2A
0.925 0.080 9 21971064 missense variant G/A;C snv 2