Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs104894313
rs104894313
TYR ; LOC107984363
7 0.807 0.160 11 89284805 missense variant C/T snv 3.8E-03; 4.0E-06 3.7E-03 0.800 1.000 4 1991 1999
dbSNP: rs104894314
rs104894314
TYR ; LOC107984363
8 0.790 0.160 11 89191205 missense variant G/A;T snv 8.0E-06; 9.2E-05 0.800 1.000 4 1991 1999
dbSNP: rs104894316
rs104894316
TYR ; LOC107984363
2 0.925 0.160 11 89284797 missense variant G/A;T snv 4.0E-06; 3.6E-05 0.700 1.000 4 1991 1999
dbSNP: rs145513733
rs145513733
TYR ; LOC107984363
1 1.000 0.160 11 89178407 missense variant C/T snv 3.5E-04 2.3E-04 0.700 1.000 4 1991 1999
dbSNP: rs61754391
rs61754391
TYR ; LOC107984363
1 1.000 0.160 11 89227924 missense variant T/C snv 0.700 1.000 4 1991 1999
dbSNP: rs61754393
rs61754393
TYR ; LOC107984363
3 0.882 0.160 11 89284853 missense variant G/A;T snv 6.0E-05; 4.0E-06 0.700 1.000 4 1991 1999
dbSNP: rs121908011
rs121908011
TYR ; LOC107984363
6 0.827 0.160 11 89227933 missense variant G/A snv 9.2E-05 3.5E-05 0.700 1.000 3 1990 2012
dbSNP: rs1126809
rs1126809
TYR ; LOC107984363
29 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 0.700 0
dbSNP: rs28940876
rs28940876
TYR ; LOC107984363
5 0.827 0.160 11 89178195 missense variant C/T snv 8.4E-05 1.7E-04 0.700 0
dbSNP: rs28940879
rs28940879
TYR ; LOC107984363
5 0.851 0.160 11 89178117 missense variant G/A;C snv 4.0E-06 0.700 0
dbSNP: rs28940881
rs28940881
TYR ; LOC107984363
16 0.776 0.200 11 89177954 start lost A/G snv 6.4E-05 5.6E-05 0.700 0
dbSNP: rs367543066
rs367543066
TYR ; LOC107984363
2 0.925 0.160 11 89178504 stop gained C/G;T snv 4.0E-06 0.700 0
dbSNP: rs61753180
rs61753180
TYR ; LOC107984363
4 0.882 0.160 11 89178093 missense variant G/A snv 1.6E-04 2.8E-04 0.700 0
dbSNP: rs61753185
rs61753185
TYR ; LOC107984363
3 0.882 0.160 11 89178183 missense variant G/A snv 8.4E-05 5.6E-05 0.700 0
dbSNP: rs61753256
rs61753256
TYR ; LOC107984363
4 0.882 0.160 11 89178299 stop gained C/A;T snv 4.0E-06; 2.4E-05 0.700 0
dbSNP: rs61754379
rs61754379
TYR ; LOC107984363
1 1.000 0.160 11 89191355 missense variant A/G snv 0.700 0
dbSNP: rs61754381
rs61754381
TYR ; LOC107984363
8 0.790 0.200 11 89227816 splice region variant T/A;C snv 9.5E-04; 8.0E-06 0.700 0
dbSNP: rs61754388
rs61754388
TYR ; LOC107984363
6 0.827 0.160 11 89227904 missense variant C/A snv 3.4E-04 5.0E-04 0.700 0
dbSNP: rs62645904
rs62645904
TYR ; LOC107984363
8 0.827 0.160 11 89191214 stop gained C/A;T snv 1.9E-04 0.700 0
dbSNP: rs62645914
rs62645914
TYR ; LOC107984363
1 1.000 0.160 11 89227954 missense variant C/G snv 4.0E-06 0.700 0
dbSNP: rs62645916
rs62645916
TYR ; LOC107984363
4 0.882 0.160 11 89284787 stop gained G/A;T snv 3.6E-05 0.700 0
dbSNP: rs63159160
rs63159160
TYR ; LOC107984363
4 0.882 0.160 11 89178602 missense variant C/G;T snv 4.0E-06; 1.8E-04 0.700 0
dbSNP: rs757754120
rs757754120
TYR ; LOC107984363
2 0.925 0.160 11 89191262 missense variant G/A snv 2.8E-05 1.4E-05 0.700 0
dbSNP: rs773970123
rs773970123
TYR ; LOC107984363
3 0.925 0.160 11 89227823 missense variant G/A;T snv 1.2E-05; 8.0E-06 0.700 0