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: rs1126809
rs1126809
TYR ; LOC107984363
29 0.683 0.320 11 89284793 missense variant G/A snv 0.18 0.18 0.700 0
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 0