Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34424986
PRKN
0.752 0.200 6 161785820 missense variant G/A;T snv 1.9E-03; 8.0E-06 10
rs1438259227
PRKN
0.827 0.080 6 162443428 missense variant T/A snv 7.0E-06 5
rs1801334
PRKN
0.851 0.040 6 161360193 missense variant C/T snv 2.5E-02 2.5E-02 4
rs1801474
PRKN
0.851 0.080 6 162201165 missense variant C/T snv 7.1E-02 5.3E-02 4
rs368134308
PRKN
0.882 0.040 6 162443356 missense variant C/A;G;T snv 3.2E-05; 2.6E-04 4
rs377591051
PRKN
0.851 0.080 6 162262651 missense variant C/T snv 4.0E-06 7.0E-06 4
rs766948045
PRKN
0.851 0.120 6 161569381 missense variant G/A snv 1.6E-05 1.4E-05 4
rs1801582
PRKN
0.925 0.120 6 161386823 missense variant C/G;T snv 0.16; 3.2E-05 3
rs9347683
PRKN ; PACRG
0.882 0.120 6 162728023 5 prime UTR variant A/C;G snv 3
rs147757966
PRKN
0.925 0.040 6 162443383 missense variant C/A;G;T snv 4.0E-06; 8.8E-05 2
rs72480422
PRKN
0.925 0.040 6 161785805 missense variant C/A;T snv 4.0E-06; 1.6E-04 2
rs1258359845
PRKN
1.000 0.040 6 161360092 synonymous variant T/C snv 1
rs1330260959
PRKN
1.000 0.040 6 161569370 missense variant A/C;T snv 4.0E-06 1
rs182893847
PRKN
1.000 0.040 6 161350125 missense variant T/C;G snv 8.0E-06; 2.9E-04 1
rs199657839
PRKN
1.000 0.040 6 161548937 missense variant G/A snv 2.4E-03 5.2E-04 1
rs56092260
PRKN
1.000 0.040 6 161386865 missense variant G/A snv 2.8E-04 1.2E-04 1
rs571092914
PRKN
1.000 0.040 6 161360181 missense variant C/A;T snv 4.0E-06; 8.0E-06 1
rs62637702
PRKN
1.000 0.040 6 161350005 3 prime UTR variant T/C snv 2.5E-02 1
rs754604402
PRKN
1.000 0.040 6 162262743 missense variant C/T snv 8.0E-06 1
rs778798543
PRKN
1.000 0.040 6 162201237 missense variant T/C snv 1.2E-05 1