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: rs1800497
rs1800497
56 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 0.030 1.000 3 2009 2017
dbSNP: rs1465781973
rs1465781973
1 1.000 0.080 11 113395026 missense variant C/T snv 2.0E-05 0.010 1.000 1 2011 2011
dbSNP: rs2734849
rs2734849
1 1.000 0.080 11 113399438 missense variant A/C;G snv 4.5E-06; 0.39 0.010 1.000 1 2009 2009
dbSNP: rs777160724
rs777160724
1 1.000 0.080 11 113396169 missense variant A/G snv 4.0E-06 0.010 1.000 1 2011 2011