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: rs200865108
rs200865108
1 1.000 0.120 17 58207143 missense variant A/G snv 4.2E-04 1.5E-03 0.700 0
dbSNP: rs201619500
rs201619500
1 1.000 0.120 17 58207104 missense variant C/T snv 2.2E-03 2.3E-03 0.700 0