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: rs748843032
rs748843032
8 0.807 0.160 4 99594840 missense variant T/C snv 4.0E-06 0.100 0.917 12 2006 2018
dbSNP: rs754736070
rs754736070
1 1.000 0.080 4 99597206 missense variant T/C snv 8.0E-06 7.0E-06 0.010 1.000 1 2006 2006