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: rs80358193
rs80358193
3 0.882 0.080 1 231374041 missense variant G/C snv 0.020 1.000 2 2008 2008
dbSNP: rs182123615
rs182123615
7 0.807 0.200 9 5070058 splice region variant T/C snv 3.6E-04 1.1E-03 0.010 1.000 1 2016 2016