Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs238406
ERCC2
0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs3218716
MYH7
0.716 0.280 14 23425316 missense variant C/A;G;T snv 4.0E-06; 2.4E-05 17
rs74315329
MYOC ; MYOCOS
0.732 0.240 1 171636338 stop gained G/A snv 1.1E-03 8.7E-04 15
rs2740574
CYP3A4
0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78 12
rs2205960
TNFSF4
0.763 0.400 1 173222336 intergenic variant G/A;T snv 9
rs104894419
LIG4
0.807 0.360 13 108208829 stop gained G/A snv 9.9E-05 7.0E-05 8
rs1555908409
RAC2
0.851 0.160 22 37232842 missense variant C/T snv 7
rs1234314
TNFSF4
0.790 0.320 1 173208253 upstream gene variant C/A;G snv 7
rs2074087
ABCC1
0.882 0.080 16 16090375 intron variant C/G snv 0.81 0.83 3
rs2278294
IMPDH1
0.882 0.080 7 128400645 non coding transcript exon variant C/T snv 0.38 3
rs11706052
IMPDH2
0.882 0.080 3 49026677 intron variant A/G snv 8.3E-02 7.6E-02 3
rs1461664423
STXBP1
1.000 0.080 9 127658446 missense variant G/A snv 7.0E-06 2
rs777018011
POLD1 ; SPIB
1.000 0.080 19 50417229 missense variant C/T snv 8.5E-06 1