Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17296479 0.851 0.040 5 81411157 non coding transcript exon variant T/A snv 9.4E-02 5
rs144551722 0.851 0.040 X 43632629 intergenic variant G/A snv 0.13 4
rs75061358 0.882 0.040 7 54848587 intergenic variant T/C;G snv 4
rs13332653 0.882 0.040 16 24578078 intergenic variant T/G snv 0.11 3
rs9933544 0.882 0.040 16 24576962 downstream gene variant A/C snv 0.29 3
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1259560536
ADAM33
1.000 0.040 20 3671756 missense variant T/C snv 7.0E-06 1
rs1402272180
AKT3
1.000 0.040 1 243637661 missense variant C/T snv 7.0E-06 1
rs2291427
ALOX5
0.925 0.040 10 45440776 intron variant A/G;T snv 2
rs2440472
AMFR
0.827 0.080 16 56402912 intron variant A/G snv 0.61 5
rs373191257
AMFR
0.827 0.080 16 56363027 missense variant T/A snv 1.6E-05 7.0E-06 5
rs3092993
ATM ; C11orf65
0.827 0.040 11 108364388 intron variant C/A snv 0.11 5
rs76151636
ATP7B
0.776 0.280 13 51944145 missense variant G/A;T snv 4.0E-06; 9.2E-04 10
rs11548193
BCAT2
0.925 0.040 19 48799813 missense variant G/A;C snv 0.14 2
rs1320938886
BLZF1
0.851 0.040 1 169376605 missense variant T/G snv 4.0E-06 4
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
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs1135401891
BRCA2
0.790 0.280 13 32332796 frameshift variant -/CT ins 7
rs11670188
BTBD2
0.925 0.040 19 2014038 non coding transcript exon variant A/G snv 0.16 2
rs373584770
CASP1
0.827 0.120 11 105030337 missense variant G/A snv 4.0E-06 7.0E-06 5
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