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: rs104894129
rs104894129
4 0.851 0.120 9 35685672 missense variant C/T snv 0.010 1.000 1 2013 2013
dbSNP: rs137853306
rs137853306
6 0.882 0.080 9 35689265 missense variant C/T snv 0.010 1.000 1 2018 2018