Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1450703683
ANOS1
1.000 0.160 X 8533018 missense variant T/C snv 1.9E-05 1
rs710190
CBX7
0.925 0.200 22 39131785 3 prime UTR variant T/C snv 0.48 1
rs877529
CBX7
1.000 0.160 22 39146287 intron variant G/A snv 0.43 1
rs961773676
SGSM3
1.000 0.160 22 40409505 missense variant G/A snv 1
rs2834167
IL10RB
0.752 0.360 21 33268483 missense variant A/G snv 0.33 0.25 10
rs765506701
IL10RB
1.000 0.160 21 33288130 missense variant G/A;C snv 4.0E-06; 8.0E-06 1
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
rs2043211
CARD8
0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 21
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 20
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 20
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 16
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 8
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 8
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 5
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 4
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 4
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 3
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 3
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 3