Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs634537
CDKN2B-AS1
0.851 0.080 9 22032153 intron variant T/G snv 0.28 6
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 17
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs1555876140
SMARCB1
22 23793671 frameshift variant -/C delins 1
rs11583706
LOC105373220
1.000 0.040 1 238358337 intron variant G/T snv 0.17 2
rs12076373
AKT3
1.000 0.040 1 243688645 intron variant G/C snv 0.20 2
rs12088062 1.000 0.040 1 244811284 intergenic variant C/T snv 0.20 2
rs10924303
LOC105373265 ; KIF26B
1.000 0.040 1 245683732 intron variant C/T snv 0.15 2
rs10924690
SMYD3
1.000 0.040 1 246320481 intron variant G/A snv 0.20 2
rs10131032
AKAP6
1.000 0.040 14 32780875 intron variant G/A snv 9.3E-02 2
rs2235573
SLC16A8
0.882 0.040 22 38081923 synonymous variant G/A snv 0.47 0.46 4
rs25489
XRCC1
0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78
rs16838813 1.000 0.040 1 4364085 intergenic variant G/A;T snv 0.11 2
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs63749993
MSH2
0.882 0.200 2 47476424 missense variant T/G snv 8
rs63750790
MSH2
1.000 0.160 2 47476425 missense variant G/A snv 3.2E-05 7.0E-06 3
rs10852606
HEATR3
0.882 0.040 16 50094961 intron variant T/A;C snv 4
rs1673041
POLD1
19 50406132 intron variant T/A;G snv 0.73 0.79 1
rs17110757
ACOT11
1.000 0.040 1 54584133 intron variant G/A snv 0.20 2
rs75061358 0.882 0.040 7 54848587 intergenic variant T/C;G snv 4
rs2252586 0.882 0.040 7 54911231 intergenic variant C/T snv 0.27 5
rs723527
EGFR
0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs59060240
EGFR
0.882 0.040 7 55080369 intron variant AA/-;A;AAA;AAAA;AAAAAAAAAAA delins 4