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: rs397516364
rs397516364
3 0.925 0.080 15 63042852 missense variant T/G snv 0.010 1.000 1 2002 2002
dbSNP: rs80358247
rs80358247
3 0.882 0.080 1 154191993 missense variant A/C snv 4.0E-06 0.010 1.000 1 2002 2002