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: rs104894159
rs104894159
5 0.827 0.080 10 62813413 missense variant G/A snv 0.010 1.000 1 2001 2001
dbSNP: rs104894161
rs104894161
6 0.807 0.080 10 62813563 missense variant G/A snv 0.010 1.000 1 2001 2001