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: rs118203347
rs118203347
1 1.000 0.120 9 132927208 missense variant T/C snv 7.0E-06 0.700 0
dbSNP: rs118203385
rs118203385
1 1.000 0.120 9 132923383 missense variant A/C;G snv 0.700 0
dbSNP: rs1323541164
rs1323541164
1 1.000 0.120 9 132921834 missense variant A/C snv 0.700 0
dbSNP: rs10234749
rs10234749
3 0.882 0.120 7 152690784 regulatory region variant T/C;G snv 0.010 1.000 1 2007 2007
dbSNP: rs1024611
rs1024611
63 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 0.010 1.000 1 2012 2012
dbSNP: rs1041983
rs1041983
15 0.732 0.240 8 18400285 synonymous variant C/T snv 0.34 0.36 0.010 1.000 1 2005 2005
dbSNP: rs1046428
rs1046428
8 0.776 0.200 14 77327940 missense variant T/A;C snv 4.0E-06; 0.81 0.010 1.000 1 2010 2010
dbSNP: rs1050450
rs1050450
43 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2014 2014
dbSNP: rs10511729
rs10511729
11 0.742 0.240 9 23557229 intron variant T/G snv 0.35 0.010 1.000 1 2014 2014
dbSNP: rs1051730
rs1051730
43 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 0.010 1.000 1 2011 2011
dbSNP: rs1051740
rs1051740
56 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2011 2011
dbSNP: rs1056827
rs1056827
24 0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 0.010 1.000 1 2013 2013
dbSNP: rs1057868
rs1057868
POR
9 0.763 0.320 7 75985688 missense variant C/T snv 0.31 0.27 0.010 1.000 1 2015 2015
dbSNP: rs1063054
rs1063054
6 0.807 0.160 8 89934373 3 prime UTR variant T/G snv 0.32 0.010 1.000 1 2010 2010
dbSNP: rs1063192
rs1063192
24 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs10719
rs10719
24 0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 0.010 1.000 1 2013 2013
dbSNP: rs10743980
rs10743980
4 0.882 0.120 12 12259861 intron variant T/A;C;G snv 0.010 1.000 1 2015 2015
dbSNP: rs10759
rs10759
4 0.851 0.160 1 163076561 3 prime UTR variant G/A;T snv 0.010 1.000 1 2013 2013
dbSNP: rs10775480
rs10775480
3 0.882 0.120 18 45737317 intron variant T/C snv 0.61 0.010 1.000 1 2013 2013
dbSNP: rs10811474
rs10811474
11 0.742 0.240 9 21114238 intergenic variant A/G snv 0.44 0.010 1.000 1 2014 2014
dbSNP: rs11077654
rs11077654
3 0.882 0.120 17 73010373 intron variant A/C snv 0.69 0.010 1.000 1 2015 2015
dbSNP: rs1109324
rs1109324
5 0.827 0.160 6 43762018 intergenic variant G/T snv 0.15 0.010 1.000 1 2007 2007
dbSNP: rs11191438
rs11191438
3 0.882 0.120 10 102878107 intron variant G/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs11191439
rs11191439
6 0.851 0.120 10 102878966 missense variant T/A;C snv 9.2E-02 0.010 1.000 1 2012 2012
dbSNP: rs11191454
rs11191454
9 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 0.010 1.000 1 2018 2018