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: rs794727993
rs794727993
1 1.000 1 160323439 missense variant C/T snv 7.0E-06 0.800 1.000 1 2015 2015
dbSNP: rs794727994
rs794727994
1 1.000 1 160314104 missense variant T/C snv 0.800 0
dbSNP: rs794727995
rs794727995
1 1.000 1 160314111 missense variant C/T snv 0.800 0
dbSNP: rs864309710
rs864309710
1 1.000 1 160323447 missense variant C/A snv 0.800 0
dbSNP: rs1557868211
rs1557868211
1 1.000 1 160314117 missense variant C/G snv 0.700 0