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: rs1438233520
rs1438233520
1 1.000 0.080 19 40844742 missense variant C/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs1801272
rs1801272
6 0.807 0.240 19 40848628 missense variant A/T snv 2.0E-02 1.8E-02 0.010 1.000 1 2011 2011
dbSNP: rs28399433
rs28399433
7 0.827 0.200 19 40850474 intron variant A/C;G;T snv 0.10; 4.4E-06 0.010 1.000 1 2011 2011
dbSNP: rs780001693
rs780001693
1 1.000 0.080 19 40846921 missense variant T/C snv 2.0E-05 0.010 1.000 1 2011 2011