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: rs1006737
rs1006737
27 0.695 0.120 12 2236129 intron variant G/A snv 0.36 0.070 1.000 7 2010 2014
dbSNP: rs794727961
rs794727961
5 0.851 0.080 12 2512979 missense variant G/A snv 0.010 1.000 1 2010 2010