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: rs1057519328
rs1057519328
1 1.000 0.200 16 3249592 missense variant G/C snv 2.1E-05 0.700 0
dbSNP: rs146597836
rs146597836
1 1.000 0.200 22 17189987 missense variant C/T snv 1.8E-03 1.6E-03 0.700 0
dbSNP: rs746055479
rs746055479
1 1.000 0.200 16 50712108 missense variant G/A;T snv 2.4E-05 0.700 0
dbSNP: rs750868279
rs750868279
1 1.000 0.200 22 17203576 missense variant G/A snv 5.2E-05 4.9E-05 0.700 0
dbSNP: rs751454741
rs751454741
1 1.000 0.200 16 3254736 missense variant C/T snv 4.0E-06 0.700 0
dbSNP: rs752615209
rs752615209
1 1.000 0.200 16 50710956 missense variant C/G;T snv 8.0E-06 0.700 0
dbSNP: rs755659290
rs755659290
1 1.000 0.200 16 3249480 missense variant T/C snv 1.2E-05 1.4E-05 0.700 0
dbSNP: rs774164456
rs774164456
1 1.000 0.200 15 77032888 missense variant G/A;C snv 2.6E-05 0.700 0
dbSNP: rs886039866
rs886039866
1 1.000 0.200 12 6333376 missense variant G/A snv 0.700 0
dbSNP: rs886040969
rs886040969
1 1.000 0.200 16 50712357 missense variant G/A snv 0.700 0
dbSNP: rs751377893
rs751377893
F5
65 0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 0.030 1.000 3 1996 2013
dbSNP: rs1217691063
rs1217691063
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.090 1.000 9 2000 2019
dbSNP: rs3743930
rs3743930
43 0.611 0.720 16 3254626 missense variant C/G;T snv 7.1E-02 0.050 0.800 5 2000 2015
dbSNP: rs61752717
rs61752717
72 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 0.040 1.000 4 2000 2015
dbSNP: rs1188383936
rs1188383936
F2
102 0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 0.030 0.667 3 2000 2013
dbSNP: rs899127658
rs899127658
F2
82 0.547 0.720 11 46739084 missense variant G/A;C snv 0.030 1.000 3 2000 2013
dbSNP: rs28940579
rs28940579
13 0.732 0.440 16 3243310 missense variant A/G;T snv 2.2E-03; 4.0E-06 0.020 1.000 2 2000 2004
dbSNP: rs1799969
rs1799969
38 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 0.030 1.000 3 2001 2016
dbSNP: rs1799983
rs1799983
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.070 0.714 7 2003 2016
dbSNP: rs1061622
rs1061622
33 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 0.010 1.000 1 2003 2003
dbSNP: rs2010963
rs2010963
82 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 0.010 1.000 1 2004 2004
dbSNP: rs231775
rs231775
115 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.030 1.000 3 2005 2014
dbSNP: rs1800450
rs1800450
26 0.662 0.640 10 52771475 missense variant C/T snv 0.14 0.11 0.020 1.000 2 2005 2017
dbSNP: rs4149584
rs4149584
24 0.683 0.440 12 6333477 missense variant C/G;T snv 4.0E-06; 1.3E-02 0.010 1.000 1 2005 2005
dbSNP: rs17235409
rs17235409
31 0.653 0.600 2 218395009 missense variant G/A;C snv 4.9E-02; 4.1E-06 0.020 1.000 2 2006 2009