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: rs201934979
rs201934979
3 0.882 0.160 15 74749838 missense variant C/T snv 8.8E-05; 8.0E-06 1.3E-04 0.010 1.000 1 2006 2006
dbSNP: rs762551
rs762551
23 0.701 0.400 15 74749576 intron variant C/A snv 0.67 0.010 1.000 1 2015 2015