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: rs2476601
rs2476601
121 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 0.030 1.000 3 2006 2011
dbSNP: rs150240657
rs150240657
3 0.925 0.120 11 47682026 missense variant G/A snv 8.7E-05 3.6E-04 0.010 1.000 1 2007 2007
dbSNP: rs1801275
rs1801275
58 0.581 0.680 16 27363079 missense variant A/G snv 0.25 0.36 0.010 1.000 1 2010 2010
dbSNP: rs1805010
rs1805010
12 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 0.010 1.000 1 2010 2010
dbSNP: rs2043211
rs2043211
29 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 0.010 1.000 1 2010 2010