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: rs770859592
rs770859592
1 1.000 0.080 9 21974599 missense variant C/T snv 1.6E-05 1.4E-05 0.010 1.000 1 2015 2015
dbSNP: rs773459232
rs773459232
1 1.000 0.080 9 21994286 missense variant C/T snv 7.0E-06 0.010 1.000 1 2015 2015