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: rs2239633
rs2239633
12 0.756 0.143 14 23119848 regulatory region variant G/A snp 0.39 0.020 1.000 2 2015 2016
dbSNP: rs3824662
rs3824662
7 0.784 0.107 10 8062245 intron variant C/A,T snp 0.17 0.020 1.000 2 2014 2016
dbSNP: rs10764338
rs10764338
1 1.000 10 22577963 intron variant T/C snp 0.83 0.010 1.000 1 2016 2016
dbSNP: rs10821936
rs10821936
8 0.784 0.107 10 61963818 intron variant C/T snp 0.72 0.010 1.000 1 2009 2009
dbSNP: rs10828317
rs10828317
5 0.821 0.250 10 22550699 missense variant snp 0.010 1.000 1 2014 2014
dbSNP: rs10994982
rs10994982
6 0.801 0.107 10 61950345 intron variant A/G snp 0.50 0.010 1.000 1 2009 2009
dbSNP: rs3731217
rs3731217
7 0.784 0.179 9 21984662 intron variant A/C,T snp 0.12 0.010 1.000 1 2016 2016
dbSNP: rs3776455
rs3776455
2 0.923 0.107 5 7896398 intron variant C/T snp 0.58 0.010 1.000 1 2014 2014
dbSNP: rs4132601
rs4132601
6 0.821 0.143 7 50402906 3 prime UTR variant T/G snp 0.25 0.010 1.000 1 2016 2016
dbSNP: rs7089424
rs7089424
4 0.878 0.107 10 61992400 intron variant T/G snp 0.29 0.010 1.000 1 2016 2016