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: rs528376963
rs528376963
1 1.000 0.120 8 38424565 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs876661335
rs876661335
1 1.000 0.120 8 38414264 missense variant C/T snv 0.700 0