Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 34
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs372043866
ERBB2
0.732 0.240 17 39727965 missense variant G/A;C;T snv 3.2E-05; 2.4E-05; 1.2E-05 18
rs121913470
ERBB2
0.776 0.200 17 39723967 missense variant T/C;G snv 13
rs749539903
ERBB2 ; MIR4728
0.827 0.120 17 39726987 missense variant G/A snv 8.4E-06 9
rs121913471
MIR4728 ; ERBB2
0.807 0.120 17 39724747 missense variant G/A;C;T snv 8
rs1801200
ERBB2
0.790 0.200 17 39723335 missense variant A/G;T snv 7
rs763193414
ERBB2
0.827 0.160 17 39707034 missense variant G/A snv 3.7E-05 4.9E-05 7
rs752295912
ERBB2
0.925 0.080 17 39710398 missense variant C/T snv 1.6E-05 6
rs759478535
ERBB2
0.851 0.080 17 39708351 missense variant A/G snv 6.8E-05 4.2E-05 6
rs28933368
ERBB2 ; MIR4728
0.851 0.080 17 39725721 missense variant G/A snv 5
rs1485579458
ERBB2
0.851 0.080 17 39723921 missense variant A/G snv 4.0E-06 4
rs767151455
ERBB2
0.925 0.080 17 39708379 missense variant C/T snv 8.0E-06 4
rs1416532705
ERBB2
0.882 0.080 17 39709435 missense variant C/T snv 4.0E-06 3
rs751074421
ERBB2
0.925 0.080 17 39715823 missense variant C/T snv 8.0E-06 3
rs777081311
ERBB2
0.925 0.080 17 39710347 missense variant T/C snv 4.0E-06 3
rs1396809633
ERBB2
0.925 0.080 17 39711979 missense variant A/G snv 7.0E-06 2
rs185670819
ERBB2
0.925 0.080 17 39708523 missense variant G/A;C snv 5.0E-04; 4.0E-06 2
rs200382130
ERBB2
0.925 0.080 17 39710388 missense variant G/T snv 2.0E-04 1.2E-04 2
rs747200104
ERBB2
0.925 0.080 17 39717388 missense variant C/A;T snv 8.0E-06 2
rs757811990
ERBB2
0.925 0.080 17 39710413 missense variant C/A;T snv 4.0E-06 2
rs778798172
ERBB2
0.925 0.080 17 39723321 missense variant C/T snv 4.0E-06 2
rs903506
ERBB2
0.925 0.080 17 39723509 intron variant G/A;T snv 0.61; 4.1E-06 2
rs2517956
ERBB2 ; PGAP3
0.925 0.080 17 39687606 intron variant G/A snv 0.62 2