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: rs397507444
rs397507444
306 0.405 0.880 1 11794407 missense variant T/G snv 0.100 1.000 11 2000 2019
dbSNP: rs1805192
rs1805192
121 0.510 0.840 3 12379739 missense variant C/G snv 0.070 0.714 7 2007 2017
dbSNP: rs266729
rs266729
37 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.030 1.000 3 2010 2015
dbSNP: rs741301
rs741301
3 0.925 0.160 7 36878390 intron variant C/T snv 0.59 0.030 1.000 3 2013 2019
dbSNP: rs7903146
rs7903146
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.030 1.000 3 2014 2018
dbSNP: rs10823108
rs10823108
2 0.925 0.160 10 67900736 intron variant G/A snv 7.1E-02 0.020 1.000 2 2017 2018
dbSNP: rs1332629192
rs1332629192
ALB
7 0.851 0.200 4 73404374 missense variant C/T snv 0.020 1.000 2 2007 2009
dbSNP: rs1411766
rs1411766
3 0.882 0.160 13 109599813 intron variant G/A;T snv 0.020 1.000 2 2010 2011
dbSNP: rs1501299
rs1501299
52 0.597 0.720 3 186853334 intron variant G/C;T snv 0.020 1.000 2 2014 2015
dbSNP: rs17446614
rs17446614
5 0.851 0.240 13 40565740 intron variant G/A snv 0.16 0.020 1.000 2 2017 2019
dbSNP: rs1799752
rs1799752
ACE
25 0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 0.020 1.000 2 2007 2009
dbSNP: rs1800625
rs1800625
39 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 0.020 1.000 2 2012 2017
dbSNP: rs1800764
rs1800764
10 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 0.020 1.000 2 2007 2009
dbSNP: rs1800795
rs1800795
140 0.494 0.840 7 22727026 intron variant C/G snv 0.71 0.020 0.500 2 2015 2019
dbSNP: rs1800796
rs1800796
74 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 0.020 0.500 2 2015 2019
dbSNP: rs1800871
rs1800871
108 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.020 1.000 2 2014 2018
dbSNP: rs1866813
rs1866813
1 1.000 0.120 3 137083096 intergenic variant A/C snv 0.14 0.020 1.000 2 2009 2013
dbSNP: rs2237897
rs2237897
6 0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 0.020 1.000 2 2010 2012
dbSNP: rs2268388
rs2268388
6 0.851 0.200 12 109205840 intron variant G/A snv 0.14 0.020 1.000 2 2013 2015
dbSNP: rs7588550
rs7588550
4 0.851 0.160 2 212304043 intron variant G/A snv 0.96 0.020 1.000 2 2012 2013
dbSNP: rs759853
rs759853
6 0.827 0.320 7 134459206 non coding transcript exon variant G/A snv 0.33 0.020 1.000 2 2006 2015
dbSNP: rs841853
rs841853
4 0.882 0.200 1 42935767 intron variant A/C snv 0.66 0.020 1.000 2 2012 2018
dbSNP: rs955333
rs955333
3 0.882 0.240 6 154626274 intergenic variant A/G snv 0.13 0.710 1.000 2 2015 2017
dbSNP: rs10019835
rs10019835
1 1.000 0.120 4 155712034 intron variant T/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs10047560
rs10047560
1 1.000 0.120 12 20452282 intron variant A/G snv 0.86 0.700 1.000 1 2011 2011