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: rs4987023
rs4987023
6 0.807 0.120 6 159692661 missense variant C/T snv 7.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs748423903
rs748423903
2 0.925 0.080 6 159688144 missense variant C/G;T snv 8.0E-06 0.010 1.000 1 2001 2001