Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1126809
LOC107984363 ; TYR
0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 29
rs28940881
LOC107984363 ; TYR
0.776 0.200 11 89177954 start lost A/G snv 6.4E-05 5.6E-05 16
rs104894314
LOC107984363 ; TYR
0.790 0.160 11 89191205 missense variant G/A;T snv 8.0E-06; 9.2E-05 8
rs61754381
LOC107984363 ; TYR
0.790 0.200 11 89227816 splice region variant T/A;C snv 9.5E-04; 8.0E-06 8
rs62645904
LOC107984363 ; TYR
0.827 0.160 11 89191214 stop gained C/A;T snv 1.9E-04 8
rs104894313
TYR ; LOC107984363
0.807 0.160 11 89284805 missense variant C/T snv 3.8E-03; 4.0E-06 3.7E-03 7
rs121908011
TYR ; LOC107984363
0.827 0.160 11 89227933 missense variant G/A snv 9.2E-05 3.5E-05 6
rs61754388
TYR ; LOC107984363
0.827 0.160 11 89227904 missense variant C/A snv 3.4E-04 5.0E-04 6
rs28940879
LOC107984363 ; TYR
0.851 0.160 11 89178117 missense variant G/A;C snv 4.0E-06 5
rs61753180
LOC107984363 ; TYR
0.882 0.160 11 89178093 missense variant G/A snv 1.6E-04 2.8E-04 4
rs62645916
LOC107984363 ; TYR
0.882 0.160 11 89284787 stop gained G/A;T snv 3.6E-05 4
rs61753256
TYR ; LOC107984363
0.882 0.160 11 89178299 stop gained C/A;T snv 4.0E-06; 2.4E-05 4
rs63159160
TYR ; LOC107984363
0.882 0.160 11 89178602 missense variant C/G;T snv 4.0E-06; 1.8E-04 4
rs1376096651
MITF
0.882 0.280 3 69964977 missense variant A/G;T snv 3