Disease: Small cell carcinoma of lung
Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519877
B2M ; PATL2
0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879
PATL2 ; B2M
0.763 0.280 15 44711548 start lost T/C;G snv 10
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 15
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 21
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16