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: rs1468885028
rs1468885028
1 1.000 0.080 1 154172960 missense variant T/G snv 4.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs199474714
rs199474714
4 0.925 0.080 1 154173113 missense variant C/T snv 0.010 1.000 1 2018 2018