Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2252586 0.882 0.040 7 54911231 intergenic variant C/T snv 0.27 5
rs75061358 0.882 0.040 7 54848587 intergenic variant T/C;G snv 4
rs12088062 1.000 0.040 1 244811284 intergenic variant C/T snv 0.20 2
rs1409785 1.000 0.040 1 74782438 intergenic variant G/A snv 0.65 2
rs16838813 1.000 0.040 1 4364085 intergenic variant G/A;T snv 0.11 2
rs17110757
ACOT11
1.000 0.040 1 54584133 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
rs12076373
AKT3
1.000 0.040 1 243688645 intron variant G/C snv 0.20 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs7572263
C2orf80
1.000 0.040 2 208186862 intron variant A/G snv 0.27 2
rs55705857
CCDC26
0.732 0.080 8 129633446 intron variant A/G snv 3.9E-02 16
rs4295627
CCDC26
0.763 0.200 8 129673211 intron variant T/G snv 0.17 11
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17 5
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
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
rs634537
CDKN2B-AS1
0.851 0.080 9 22032153 intron variant T/G snv 0.28 6
rs12021720
DBT
0.925 0.160 1 100206504 missense variant T/A;C snv 0.92 3
rs11979158
EGFR
0.882 0.040 7 55091656 intron variant A/G;T snv 0.20 5
rs59060240
EGFR
0.882 0.040 7 55080369 intron variant AA/-;A;AAA;AAAA;AAAAAAAAAAA delins 4
rs723527
EGFR
0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs1801591
ETFA
0.882 0.040 15 76286421 missense variant G/A snv 7.4E-02 6.4E-02 4
rs77633900
ETFA
1.000 0.040 15 76246118 intron variant G/C snv 6.3E-02 2