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: rs758119182
rs758119182
1 1.000 0.040 10 68210291 missense variant T/C snv 0.010 1.000 1 2015 2015
dbSNP: rs794729072
rs794729072
1 1.000 0.040 10 68166581 missense variant G/A snv 4.0E-06 7.0E-06 0.010 1.000 1 2015 2015