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: rs11599176
rs11599176
2 0.925 0.080 10 67894017 intron variant A/G snv 0.11 0.010 1.000 1 2018 2018
dbSNP: rs1801282
rs1801282
131 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 1.000 1 2010 2010
dbSNP: rs1805192
rs1805192
121 0.510 0.840 3 12379739 missense variant C/G snv 0.010 1.000 1 2010 2010
dbSNP: rs33957861
rs33957861
3 0.882 0.160 10 67887218 intron variant C/T snv 0.11 0.010 1.000 1 2018 2018
dbSNP: rs35689145
rs35689145
1 1.000 0.080 10 67900009 intron variant G/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs3816873
rs3816873
9 0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 0.010 1.000 1 2009 2009