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: rs10994982
rs10994982
7 0.790 0.120 10 61950345 intron variant A/G snv 0.49 0.020 1.000 2 2009 2014
dbSNP: rs2239633
rs2239633
12 0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 0.020 1.000 2 2015 2015
dbSNP: rs3824662
rs3824662
11 0.752 0.320 10 8062245 intron variant C/A;T snv 0.020 1.000 2 2013 2015
dbSNP: rs10764338
rs10764338
1 1.000 10 22577963 intron variant T/C snv 0.82 0.010 1.000 1 2015 2015
dbSNP: rs10821936
rs10821936
11 0.742 0.200 10 61963818 intron variant C/T snv 0.69 0.010 1.000 1 2009 2009
dbSNP: rs10828317
rs10828317
9 0.776 0.280 10 22550699 missense variant T/C snv 0.010 1.000 1 2013 2013
dbSNP: rs2811712
rs2811712
5 0.882 0.080 9 21998036 intron variant G/A snv 0.85 0.010 1.000 1 2017 2017
dbSNP: rs3731217
rs3731217
10 0.763 0.320 9 21984662 intron variant A/C;T snv 0.010 1.000 1 2015 2015
dbSNP: rs3776455
rs3776455
2 0.925 0.120 5 7896398 intron variant C/T snv 0.58 0.010 1.000 1 2013 2013
dbSNP: rs4132601
rs4132601
9 0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 0.010 1.000 1 2015 2015
dbSNP: rs7089424
rs7089424
10 0.752 0.200 10 61992400 intron variant T/G snv 0.32 0.010 1.000 1 2015 2015
dbSNP: rs76925697
rs76925697
2 0.925 0.120 9 81132456 regulatory region variant A/T snv 3.4E-02 0.010 1.000 1 2019 2019
dbSNP: rs886285
rs886285
2 0.925 0.120 5 132429514 intron variant T/C snv 0.57 0.010 1.000 1 2019 2019