Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs10814325
RECK
0.827 0.200 9 36036597 upstream gene variant T/A;C;G snv 7
rs10817938
PTCSC2
0.882 0.080 9 97700127 non coding transcript exon variant T/C snv 3.2E-02 5
rs10964859
IFNW1
9 21140673 3 prime UTR variant C/A;G snv 1
rs10964862 9 21151554 intergenic variant C/A;G snv 1
rs11016879
MGMT
0.882 0.040 10 129691518 intron variant A/C;G snv 0.66 4
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs11121704
MTOR
1 11233902 intron variant C/A;T snv 3
rs112445441
KRAS
0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs11246050
NLRP6
1.000 0.080 11 284257 synonymous variant G/A;C snv 0.16; 4.0E-06 2
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1131691036
TP53
0.851 0.080 17 7675207 frameshift variant GCA/CC delins 8
rs1131692237
ERBB2 ; MIR4728
1.000 0.040 17 39725161 missense variant T/G snv 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs1137282
KRAS
0.851 0.120 12 25209843 missense variant A/G;T snv 0.19 5
rs115160714
TOPBP1
0.807 0.200 3 133601021 3 prime UTR variant G/A snv 5.8E-03 9
rs11547328
CDK4
0.701 0.360 12 57751648 missense variant G/A;T snv 4.0E-06 27
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11549467
HIF1A ; HIF1A-AS3
0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs1156560901
CDK15
2 201880120 missense variant A/G snv 1.4E-05 2
rs115785973
SOCS3
0.925 0.080 17 78357871 3 prime UTR variant C/G;T snv 3
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111