Source: ALL
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
rs4693608
HPSE
0.827 0.200 4 83320204 intron variant G/A;C snv 6
rs6535455
HPSE
0.851 0.160 4 83310951 intron variant T/A;C snv 4
rs17501560 1.000 0.160 7 81786467 intergenic variant A/G snv 0.13 1
rs12584389 0.925 0.200 13 79801869 upstream gene variant T/C snv 4.4E-02 2
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
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 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs730882018
TP53
0.851 0.320 17 7676153 frameshift variant G/-;GG delins 5
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 16
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57