Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs11553473
UBE2I
0.882 0.080 16 1314299 missense variant G/A snv 3
rs7187167 1.000 0.040 16 1299208 upstream gene variant T/C snv 0.69 2
rs121908690
RAD54L ; LRRC41
0.925 0.080 1 46267540 missense variant G/A snv 1.4E-05 2
rs371228501
EGFR
1.000 0.040 7 55191740 missense variant C/T snv 6.8E-05 1.2E-04 1