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: rs10012
rs10012
8 0.769 0.214 2 38075247 missense variant G/C snp 0.31 0.36 0.020 0.500 2 2011 2015
dbSNP: rs1011970
rs1011970
13 0.715 0.286 9 22062135 intron variant G/T snp 0.22 0.700 1 2017 2017
dbSNP: rs10203853
rs10203853
3 0.923 0.071 2 233778772 intron variant A/G,T snp 0.42 0.010 1.000 1 2014 2014
dbSNP: rs10204525
rs10204525
8 0.769 0.321 2 241850169 3 prime UTR variant C/T snp 0.21 0.010 1.000 1 2017 2017
dbSNP: rs1028166
rs1028166
1 1.000 0.071 4 181892145 intron variant G/A snp 0.73 0.700 1 2015 2015
dbSNP: rs10318
rs10318
3 0.878 0.071 15 32733778 3 prime UTR variant C/T snp 0.17 0.010 1.000 1 2014 2014
dbSNP: rs1035209
rs1035209
2 0.923 0.071 10 99585609 intergenic variant C/T snp 0.16 0.700 1 2015 2015
dbSNP: rs10380
rs10380
7 0.784 0.179 5 7897078 missense variant C/T snp 0.16 0.16 0.010 1.000 1 2011 2011
dbSNP: rs10411210
rs10411210
4 0.878 0.071 19 33041394 intron variant C/T snp 0.20 0.710 1.000 2 2008 2016
dbSNP: rs10414971
rs10414971
1 1.000 0.071 19 12351131 missense variant G/A snp 1.9E-03 7.5E-03 0.700 1 2006 2006
dbSNP: rs1042028
rs1042028
20 0.685 0.321 16 28606193 missense variant C/T snp 0.22 0.31 0.020 1.000 2 2006 2011
dbSNP: rs1042522
rs1042522
56 0.563 0.643 17 7676154 stop gained G/C,T snp 0.67 0.62 0.020 0.500 2 2010 2018
dbSNP: rs1042821
rs1042821
11 0.756 0.214 2 47783349 missense variant G/A,C snp 0.18; 8.6E-06 0.19 0.020 0.500 2 2009 2018
dbSNP: rs1043397364
rs1043397364
1 1.000 0.071 16 89637349 missense variant G/A,T snp 2.8E-05; 4.0E-06 3.2E-05; 3.2E-05 0.700 1 2006 2006
dbSNP: rs1045485
rs1045485
26 0.652 0.393 2 201284866 missense variant G/A,C,T snp 4.0E-06; 9.0E-02 3.2E-05; 9.8E-02 0.010 < 0.001 1 2008 2008
dbSNP: rs1045642
rs1045642
108 0.520 0.714 7 87509329 synonymous variant A/G,T snp 0.50 0.56 0.070 1.000 7 2008 2018
dbSNP: rs10457678
rs10457678
2 1.000 0.071 6 138801103 intron variant A/G snp 0.19 0.700 1 2016 2016
dbSNP: rs1047781
rs1047781
10 0.769 0.179 19 48703374 missense variant A/T snp 3.6E-02 2.3E-02 0.010 1.000 1 2015 2015
dbSNP: rs104886003
rs104886003
52 0.580 0.393 3 179218303 missense variant G/A,C snp 4.0E-06 0.700 0
dbSNP: rs104893751
rs104893751
4 0.846 0.214 3 9750423 missense variant G/A,C snp 2.2E-03; 4.0E-06 1.8E-03 0.010 1.000 1 2011 2011
dbSNP: rs1048943
rs1048943
53 0.572 0.571 15 74720644 missense variant T/C snp 0.11 5.0E-02 0.030 1.000 3 2008 2011
dbSNP: rs1048945
rs1048945
4 0.846 0.107 14 20456008 missense variant G/C snp 2.1E-02 2.2E-02 0.010 1.000 1 2011 2011
dbSNP: rs10490920
rs10490920
2 0.923 0.071 10 87925886 intron variant T/C snp 0.13 0.010 1.000 1 2014 2014
dbSNP: rs1049434
rs1049434
3 0.878 0.107 1 112913924 missense variant A/T snp 0.59 0.66 0.010 1.000 1 2015 2015
dbSNP: rs10505477
rs10505477
12 0.744 0.179 8 127395198 intron variant A/G snp 0.41 0.720 1.000 6 2007 2017