Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs3804099
TLR2
0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 40
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs1445081098
COMT ; MIR4761
0.724 0.480 22 19963746 missense variant G/C snv 4.0E-06 17
rs760025060
CYP1B1 ; CYP1B1-AS1
0.776 0.200 2 38074936 missense variant C/T snv 10
rs1456315
PRNCR1 ; PCAT1 ; CASC19
0.790 0.200 8 127091692 non coding transcript exon variant T/A;C snv 9
rs11655505
NBR2 ; BRCA1
0.776 0.160 17 43126360 intron variant G/A snv 0.31 8
rs999737
RAD51B
0.776 0.200 14 68567965 intron variant C/T snv 0.16 8
rs7463708
PCAT1 ; CASC19 ; PRNCR1
0.807 0.120 8 127091810 non coding transcript exon variant G/T snv 0.27 7
rs6504950
STXBP4
0.807 0.120 17 54979110 intron variant G/A snv 0.29 7
rs1314913
RAD51B
0.807 0.120 14 68232877 intron variant C/T snv 0.13 6
rs2588809
RAD51B
0.807 0.160 14 68193711 intron variant T/C snv 0.80 6
rs756706958
BRAF
0.925 0.080 7 140776967 missense variant T/C snv 2
rs769492487
MIR4761 ; COMT
0.925 0.080 22 19964287 synonymous variant G/A;T snv 8.0E-06; 8.0E-06 2