Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 3
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 3
rs1057519832
PLCG2
1.000 0.120 16 81928578 missense variant A/C;G;T snv 1
rs1057519831
PLCG2
1.000 0.120 16 81912655 missense variant C/T snv 1
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 1
rs1057519997
TP53
0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 16
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 13
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 11
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 8
rs876659675
TP53
0.807 0.280 17 7674199 missense variant A/C;G;T snv 7
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 3
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 29