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: rs1341667
rs1341667
2 0.923 0.036 10 68882104 missense variant T/C snp 0.62 0.59 0.030 0.667 3 2007 2011
dbSNP: rs1799889
rs1799889
12 0.734 0.321 7 101126430 intergenic variant A/G snp 0.020 1.000 2 2013 2013
dbSNP: rs1799983
rs1799983
138 0.475 0.786 7 150999023 missense variant T/A,G snp 0.75 0.76 0.020 0.500 2 2007 2010
dbSNP: rs10497025
rs10497025
1 1.000 0.036 2 147904633 intron variant C/G snp 0.18 0.010 1.000 1 2009 2009
dbSNP: rs1137101
rs1137101
41 0.605 0.679 1 65592830 missense variant A/G snp 0.51 0.53 0.010 1.000 1 2010 2010
dbSNP: rs13430086
rs13430086
1 1.000 0.036 2 147929492 3 prime UTR variant A/T snp 0.32 0.010 1.000 1 2009 2009
dbSNP: rs1424954
rs1424954
1 1.000 0.036 2 147843225 intergenic variant G/A snp 0.33 0.010 1.000 1 2015 2015
dbSNP: rs142724505
rs142724505
2 0.923 0.107 8 144080528 missense variant G/A snp 1.8E-03 1.2E-03 0.010 1.000 1 2010 2010
dbSNP: rs153109
rs153109
11 0.744 0.357 16 28507775 intron variant T/C snp 0.45 0.010 1.000 1 2016 2016
dbSNP: rs17855750
rs17855750
4 0.878 0.107 16 28503907 missense variant A/C,T snp 6.4E-02; 4.0E-06 5.7E-02 0.010 1.000 1 2016 2016
dbSNP: rs2059806
rs2059806
3 0.923 0.107 19 7166365 synonymous variant C/G,T snp 4.0E-06; 0.26 3.2E-05; 0.23 0.010 1.000 1 2017 2017
dbSNP: rs2507800
rs2507800
3 1.000 0.036 8 107250441 3 prime UTR variant T/A snp 0.34; 1.5E-02 0.010 1.000 1 2012 2012
dbSNP: rs5370
rs5370
17 0.715 0.250 6 12296022 missense variant G/T snp 0.23 0.21 0.010 < 0.001 1 2001 2001