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
rs1477349434
ERBB2
1.000 17 39715520 missense variant G/C snv 4.0E-06 1
rs977818812
ERBB2
1.000 0.040 17 39723608 missense variant A/T snv 3
rs1416951791
ERBB2
1.000 0.040 17 39708413 missense variant G/C snv 4.0E-06 2
rs896171398
ERBB2
1.000 0.040 17 39709846 missense variant G/A;C snv 1.6E-05 2
rs1131692237
ERBB2 ; MIR4728
1.000 0.040 17 39725161 missense variant T/G snv 1
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
rs61552325
ERBB2
0.882 0.080 17 39727784 missense variant C/G snv 5
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
rs767151455
ERBB2
0.925 0.080 17 39708379 missense variant C/T snv 8.0E-06 4
rs564064363
ERBB2
0.851 0.080 17 39706998 missense variant G/A;C snv 1.3E-05 4
rs777081311
ERBB2
0.925 0.080 17 39710347 missense variant T/C snv 4.0E-06 3
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
rs1238981206
ERBB2 ; MIR4728
0.925 0.080 17 39724828 missense variant G/A snv 4.0E-06 3
rs1057519857
ERBB2 ; MIR4728
0.882 0.080 17 39724772 missense variant T/C snv 3