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: rs6295
rs6295
40 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.070 1.000 7 2008 2019
dbSNP: rs1800041
rs1800041
4 0.882 0.120 5 63961673 missense variant G/A snv 1.8E-03 5.3E-04 0.010 1.000 1 2004 2004
dbSNP: rs1800044
rs1800044
8 0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03 0.010 1.000 1 2009 2009