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: rs768047421
rs768047421
HTT
1 1.000 4 3131647 missense variant C/T snv 8.1E-05 3.5E-05 0.800 0
dbSNP: rs1060505028
rs1060505028
HTT
1 1.000 4 3229927 missense variant T/A snv 0.700 0
dbSNP: rs1085307052
rs1085307052
HTT
1 1.000 4 3229928 missense variant T/A snv 0.700 0
dbSNP: rs34315806
rs34315806
HTT
1 1.000 4 3160307 missense variant C/T snv 5.6E-03 2.4E-02 0.700 0