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: rs1050851
rs1050851
1 1.000 0.071 14 35403720 synonymous variant G/A snp 0.17 0.15 0.010 1.000 1 2016 2016
dbSNP: rs12457893
rs12457893
1 1.000 0.071 18 63258928 intron variant A/C snp 0.40 0.010 1.000 1 2012 2012
dbSNP: rs1799983
rs1799983
138 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 0.010 1.000 1 2016 2016
dbSNP: rs2233417
rs2233417
1 1.000 0.071 14 35402888 intron variant C/T snp 0.14 0.13 0.010 1.000 1 2016 2016
dbSNP: rs2276415
rs2276415
6 0.878 0.143 11 77590296 missense variant G/A snp 0.14 0.13 0.010 < 0.001 1 2016 2016
dbSNP: rs41507953
rs41507953
7 0.821 0.143 8 27500988 missense variant A/G snp 8.7E-02 0.13 0.010 1.000 1 2017 2017
dbSNP: rs782818582
rs782818582
3 0.878 0.143 9 133456116 stop gained C/T snp 1.2E-05 0.010 1.000 1 2006 2006
dbSNP: rs8094315
rs8094315
1 1.000 0.071 18 63268814 intron variant A/G snp 0.19 0.010 1.000 1 2012 2012