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: rs104895097
rs104895097
1 0.925 0.040 16 3243205 missense variant C/T snv 2.0E-04 1.1E-04 0.850 1.000 5 1998 2020
dbSNP: rs61732874
rs61732874
1 0.925 0.040 16 3243257 missense variant C/A;T snv 1.8E-03; 1.2E-05 0.820 1.000 2 1998 2018
dbSNP: rs104895076
rs104895076
1 1.000 0.040 16 3254625 missense variant T/A;G snv 7.7E-05; 4.3E-06 0.710 1.000 1 2017 2017
dbSNP: rs104895193
rs104895193
1 1.000 0.040 16 3244284 missense variant T/A snv 0.010 1.000 1 2014 2014
dbSNP: rs1274043842
rs1274043842
1 1.000 0.040 16 3248950 missense variant C/T snv 7.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs141829974
rs141829974
C5
1 1.000 0.040 9 121037923 synonymous variant G/A snv 2.6E-04 8.0E-04 0.010 1.000 1 2010 2010
dbSNP: rs190405488
rs190405488
1 1.000 0.040 16 3249609 missense variant C/G snv 2.0E-05 0.010 1.000 1 2015 2015
dbSNP: rs368859219
rs368859219
1 1.000 0.040 6 137881228 missense variant G/A;T snv 7.4E-05; 8.2E-06 0.010 1.000 1 2020 2020
dbSNP: rs4804049
rs4804049
1 1.000 0.040 19 47320227 synonymous variant T/A;C snv 4.0E-06; 0.99 0.010 1.000 1 2010 2010
dbSNP: rs75977701
rs75977701
1 1.000 0.040 16 3254158 missense variant C/T snv 4.6E-03 3.2E-03 0.010 1.000 1 2012 2012
dbSNP: rs11466024
rs11466024
2 0.925 0.080 16 3249468 missense variant C/A;T snv 1.6E-05; 1.3E-02 0.840 1.000 4 1999 2016
dbSNP: rs1440063914
rs1440063914
2 0.925 0.080 2 8779781 missense variant T/C snv 0.020 1.000 2 2001 2004
dbSNP: rs104895081
rs104895081
2 0.925 0.080 16 3254268 missense variant G/A snv 1.6E-04 1.1E-04 0.810 1.000 1 2010 2015
dbSNP: rs767006697
rs767006697
2 0.925 0.080 16 3254658 frameshift variant C/- delins 0.010 < 0.001 1 2001 2001
dbSNP: rs104895105
rs104895105
6 0.851 0.120 16 3247171 missense variant G/A snv 0.010 1.000 1 2004 2004
dbSNP: rs11466018
rs11466018
5 0.827 0.200 16 3254739 missense variant A/G snv 6.6E-03 2.2E-03 0.730 1.000 3 2008 2013
dbSNP: rs79071878
rs79071878
7 0.827 0.240 5 132680652 intron variant ATGAAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGACGATGGTGGCGTGGACAGAATGAAGCAAGATGGCCTGTTGGGAGGCTACCACAGTAAACCAGGCTAGAGATGATGGTGGCGTGGACAGAAT/- del 0.020 < 0.001 2 2016 2018
dbSNP: rs11466023
rs11466023
6 0.827 0.320 16 3249586 missense variant G/A;T snv 1.5E-02; 4.0E-05 0.860 1.000 6 2008 2017
dbSNP: rs104895094
rs104895094
5 0.851 0.320 16 3243403 missense variant T/A;C snv 8.0E-06; 5.2E-03 0.810 1.000 1 1998 2016
dbSNP: rs28940578
rs28940578
14 0.716 0.400 16 3243405 missense variant C/T snv 1.4E-04 6.3E-05 0.900 1.000 14 1997 2017
dbSNP: rs28940579
rs28940579
10 0.732 0.440 16 3243310 missense variant A/G;T snv 2.2E-03; 4.0E-06 0.900 1.000 11 1997 2019
dbSNP: rs224222
rs224222
15 0.724 0.440 16 3254463 missense variant C/T snv 0.24 0.21 0.080 1.000 8 2007 2019
dbSNP: rs4149584
rs4149584
24 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.020 1.000 2 2008 2010
dbSNP: rs1289543302
rs1289543302
12 0.763 0.440 7 87536472 missense variant C/T snv 0.010 1.000 1 2014 2014
dbSNP: rs2234663
rs2234663
14 0.716 0.480 2 113130529 intron variant ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC/-;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC delins 0.010 < 0.001 1 2016 2016