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: rs104894314
rs104894314
TYR ; LOC107984363
8 0.790 0.160 11 89191205 missense variant G/A;T snv 8.0E-06; 9.2E-05 0.010 1.000 1 1991 1991
dbSNP: rs28940876
rs28940876
TYR ; LOC107984363
5 0.827 0.160 11 89178195 missense variant C/T snv 8.4E-05 1.7E-04 0.010 1.000 1 1991 1991