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: rs9833094
rs9833094
2 1.000 0.071 3 100872081 intron variant C/A,T snp 0.33 0.700 1 2014 2014
dbSNP: rs12746200
rs12746200
5 0.878 0.107 1 186880054 intron variant A/G snp 6.7E-02 0.010 1.000 1 2016 2016
dbSNP: rs147080557
rs147080557
5 0.878 0.107 19 53810777 missense variant G/A,C snp 3.6E-05; 4.0E-06 6.4E-05 0.010 1.000 1 2013 2013
dbSNP: rs1805034
rs1805034
6 0.821 0.179 18 62360008 missense variant C/T snp 0.54 0.56 0.010 1.000 1 2016 2016
dbSNP: rs2228246
rs2228246
1 1.000 0.071 20 41163423 missense variant A/G snp 0.14 0.16 0.010 1.000 1 2016 2016
dbSNP: rs35211496
rs35211496
3 0.878 0.107 18 62354528 missense variant C/T snp 0.12 0.11 0.010 1.000 1 2016 2016