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: rs1057519766
rs1057519766
5 0.851 0.080 13 28028203 missense variant G/C;T snv 0.010 1.000 1 2016 2016
dbSNP: rs751689316
rs751689316
4 0.925 0.080 3 169131510 missense variant C/T snv 1.2E-05 0.010 1.000 1 2008 2008
dbSNP: rs767464424
rs767464424
3 0.925 0.080 2 37222420 frameshift variant T/- delins 4.2E-06 0.010 1.000 1 2016 2016
dbSNP: rs777017502
rs777017502
3 0.925 0.080 2 37222420 missense variant T/C;G snv 4.2E-06; 4.2E-06 0.010 1.000 1 2016 2016
dbSNP: rs2230724
rs2230724
4 0.851 0.120 9 5081780 synonymous variant G/A snv 0.53 0.62 0.010 1.000 1 2012 2012
dbSNP: rs1325757098
rs1325757098
6 0.827 0.160 16 71576223 missense variant C/T snv 8.0E-06 7.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs62527607
rs62527607
5 0.827 0.160 8 103141321 non coding transcript exon variant G/T snv 0.14 0.010 1.000 1 2017 2017
dbSNP: rs8073069
rs8073069
7 0.807 0.200 17 78213692 upstream gene variant G/C snv 0.33 0.010 < 0.001 1 2018 2018
dbSNP: rs111033563
rs111033563
8 0.776 0.240 6 26092916 missense variant A/C snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs11978267
rs11978267
9 0.763 0.240 7 50398606 intron variant A/G snv 0.25 0.010 1.000 1 2014 2014
dbSNP: rs1470755915
rs1470755915
10 0.776 0.240 8 92005229 missense variant C/A snv 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs1799929
rs1799929
11 0.776 0.240 8 18400484 synonymous variant C/T snv 0.36 0.36 0.010 1.000 1 2019 2019
dbSNP: rs2239633
rs2239633
12 0.742 0.240 14 23119848 upstream gene variant G/A snv 0.38 0.010 1.000 1 2015 2015
dbSNP: rs4132601
rs4132601
9 0.763 0.240 7 50402906 3 prime UTR variant T/G snv 0.25 0.010 1.000 1 2014 2014
dbSNP: rs797045145
rs797045145
6 0.807 0.240 6 26091479 stop gained G/A snv 0.010 1.000 1 2005 2005
dbSNP: rs927698341
rs927698341
10 0.776 0.240 8 92005280 synonymous variant C/A snv 4.0E-06 2.8E-05 0.010 1.000 1 2011 2011
dbSNP: rs1532268
rs1532268
12 0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 0.010 1.000 1 2012 2012
dbSNP: rs387906659
rs387906659
14 0.742 0.280 19 40257052 stop gained C/A;T snv 0.010 1.000 1 2008 2008
dbSNP: rs559063155
rs559063155
14 0.732 0.280 2 197402110 stop gained T/A;C;G snv 9.0E-05 0.010 1.000 1 2017 2017
dbSNP: rs9904341
rs9904341
20 0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 0.010 1.000 1 2018 2018
dbSNP: rs1239681664
rs1239681664
15 0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs2295080
rs2295080
20 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 0.010 1.000 1 2016 2016
dbSNP: rs397514606
rs397514606
14 0.763 0.320 1 243695714 missense variant C/T snv 0.010 1.000 1 2008 2008
dbSNP: rs35201683
rs35201683
HFE
12 0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 0.010 1.000 1 2005 2005
dbSNP: rs562015640
rs562015640
16 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 0.010 1.000 1 2011 2011