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: rs773919809
rs773919809
13 0.763 0.200 10 129766957 missense variant C/T snv 2.0E-05 0.030 1.000 3 2008 2012
dbSNP: rs7087131
rs7087131
1 1.000 0.080 10 129676210 intron variant G/A snv 0.15 0.010 1.000 1 2009 2009