Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069416
CDKN2B ; CDKN2B-AS1
0.925 0.040 9 22010005 intron variant T/A;G snv 3
rs2383205
CDKN2B-AS1
0.925 0.080 9 22060936 intron variant A/C;G snv 3
rs10511701
CDKN2B-AS1
9 22112600 intron variant T/A;C snv 2
rs10757267
CDKN2B-AS1
1.000 0.040 9 22052811 intron variant G/A;C;T snv 2
rs10811651
CDKN2B-AS1
1.000 0.040 9 22067831 intron variant G/A;C snv 2
rs10978777 1.000 0.080 9 107268309 intergenic variant G/A;C snv 2
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2
rs12040333
ST3GAL3
1.000 0.080 1 43848369 intron variant G/A;C snv 2
rs1333039
CDKN2B-AS1
1.000 0.040 9 22065658 splice region variant G/A;C;T snv 2
rs1360590
CDKN2B-AS1
1.000 0.040 9 22041444 intron variant T/C;G snv 2
rs16879003
ATXN1
1.000 0.080 6 16745008 intron variant T/C;G snv 2
rs16939881
ALDH1A2 ; AQP9
15 58179780 intron variant G/C;T snv 2
rs2106119
CDKN2B-AS1
1.000 0.040 9 22017551 intron variant A/G;T snv 2
rs3809346
COL4A1 ; COL4A2
1.000 0.080 13 110308596 intron variant G/A;C snv 2
rs448792
FRY
1.000 0.080 13 32103287 intron variant T/A;C snv 2
rs4977575
CDKN2B-AS1
1.000 0.040 9 22124745 intron variant C/G;T snv 2
rs543554
FRY
1.000 0.080 13 32127501 intron variant A/G;T snv 2
rs543830
CDKN2B-AS1
1.000 0.040 9 22026640 intron variant A/C;T snv 2
rs6506900
LOC105372049
1.000 0.080 18 31226433 intergenic variant A/C;G snv 2
rs6606859
GABRG3
1.000 0.080 15 27032254 intron variant C/A;T snv 2
rs6754498
LOC107985783
1.000 0.080 2 185953121 non coding transcript exon variant A/C;G;T snv 2
rs679038
CDKN2B-AS1
1.000 0.040 9 22029081 intron variant G/A;T snv 2
rs7027048
CDKN2B-AS1
1.000 0.040 9 22053710 intron variant A/G;T snv 2
rs7442201
NSG1
1.000 0.080 4 4360022 intron variant A/C;G snv 2
rs75629841
MTSS1
1.000 0.080 8 124714135 intron variant G/A;T snv 2