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: rs2675703
rs2675703
1 1.000 0.040 10 86654812 missense variant C/T snv 0.10 0.10 0.020 1.000 2 2009 2018
dbSNP: rs1079610
rs1079610
1 1.000 0.040 10 86662359 missense variant C/T snv 0.70 0.70 0.010 1.000 1 2018 2018