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: rs1265416900
rs1265416900
2 0.925 0.040 14 92932783 missense variant C/T snv 0.010 1.000 1 2013 2013
dbSNP: rs1456371000
rs1456371000
2 0.925 0.040 14 92931642 missense variant C/T snv 0.010 1.000 1 2013 2013