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: rs1800470
rs1800470
107 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 0.010 < 0.001 1 2018 2018
dbSNP: rs2241718
rs2241718
4 0.882 0.040 19 41323701 3 prime UTR variant G/A snv 0.15 0.010 1.000 1 2014 2014