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: rs10814083
rs10814083
3 0.882 0.160 9 34256349 synonymous variant C/T snv 0.40 0.34 0.010 1.000 1 2010 2010
dbSNP: rs74315414
rs74315414
5 0.882 0.200 20 4699533 missense variant C/A;T snv 4.0E-06 0.010 1.000 1 2008 2008