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: rs10514611
rs10514611
2 0.923 0.071 16 85921636 3 prime UTR variant C/T snp 0.24 0.010 1.000 1 2014 2014
dbSNP: rs1801131
rs1801131
49 0.599 0.607 1 11794419 missense variant T/G snp 0.29 0.26 0.010 1.000 1 2014 2014
dbSNP: rs2032582
rs2032582
54 0.602 0.500 7 87531302 missense variant A/C,T snp 0.54; 3.8E-02 0.64; 2.5E-02 0.010 < 0.001 1 2014 2014
dbSNP: rs2268276
rs2268276
2 0.923 0.036 21 34808717 intron variant G/A snp 0.37 0.010 1.000 1 2017 2017
dbSNP: rs35602083
rs35602083
3 0.878 0.036 13 28049450 missense variant C/T snp 1.7E-02 1.7E-02 0.010 1.000 1 2006 2006
dbSNP: rs768942227
rs768942227
1 1.000 0.036 19 17832629 missense variant A/G snp 0.010 1.000 1 2016 2016