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: rs516514
rs516514
1 1.000 0.040 18 36681085 intron variant C/T snv 0.49 0.710 1.000 1 2013 2013
dbSNP: rs2303510
rs2303510
1 1.000 0.040 18 36744128 missense variant G/A snv 0.34 0.35 0.010 1.000 1 2013 2013