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: rs747504890
rs747504890
3 0.925 0.080 18 63318285 missense variant C/T snv 2.4E-05 0.030 1.000 3 2002 2004
dbSNP: rs2279115
rs2279115
18 0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv 0.010 1.000 1 2017 2017