Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs372811772
ERBB2
17 39708435 synonymous variant C/T snv 8.0E-06 2.1E-05 2
rs1308088661
ERBB2
17 39727880 missense variant G/A snv 4.0E-06 2
rs1457127715
ERBB2
17 39715810 missense variant G/A;C snv 4.0E-06 2
rs542027040
MIR4728 ; ERBB2
17 39724864 missense variant C/T snv 1.2E-05 1
rs772604432
ERBB2
17 39727376 missense variant G/A;C snv 1
rs959969530
ERBB2
17 39727763 missense variant G/A snv 1
rs369293607
ERBB2
17 39707018 synonymous variant G/A snv 1
rs763371007
ERBB2
17 39709441 missense variant G/A snv 4.4E-05 4.9E-05 1
rs1136201
ERBB2
0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 33
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
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 6
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 3
rs121913470
ERBB2
0.776 0.200 17 39723967 missense variant T/C;G snv 6
rs1801200
ERBB2
0.790 0.200 17 39723335 missense variant A/G;T snv 7
rs1057519738
MIR4728 ; ERBB2
0.790 0.160 17 39725079 missense variant G/A snv 4.0E-06 3
rs121913471
MIR4728 ; ERBB2
0.807 0.120 17 39724747 missense variant G/A;C;T snv 5
rs1057519890
ERBB2
0.807 0.200 17 39723966 missense variant T/A snv 1
rs749539903
ERBB2 ; MIR4728
0.827 0.120 17 39726987 missense variant G/A snv 8.4E-06 9
rs763193414
ERBB2
0.827 0.160 17 39707034 missense variant G/A snv 3.7E-05 4.9E-05 7
rs121913468
ERBB2
0.827 0.160 17 39724008 missense variant G/A;C;T snv 2
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 4
rs1485579458
ERBB2
0.851 0.080 17 39723921 missense variant A/G snv 4.0E-06 4
rs564064363
ERBB2
0.851 0.080 17 39706998 missense variant G/A;C snv 1.3E-05 4