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: rs1003342
rs1003342
1 22 30174033 intron variant A/G snv 0.45 0.700 1.000 1 2015 2015
dbSNP: rs1004819
rs1004819
9 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.020 1.000 2 2007 2012
dbSNP: rs10051722
rs10051722
2 1.000 0.040 5 130768383 intron variant A/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs10061469
rs10061469
1 5 73222321 intron variant T/C snv 0.37 0.700 1.000 1 2015 2015
dbSNP: rs10063949
rs10063949
4 0.882 0.080 5 139383837 intron variant T/C snv 0.48 0.010 1.000 1 2014 2014
dbSNP: rs10065172
rs10065172
8 0.790 0.200 5 150848436 synonymous variant C/T snv 0.17 0.21 0.010 1.000 1 2011 2011
dbSNP: rs10065637
rs10065637
2 1.000 0.040 5 56143024 intron variant C/T snv 0.15 0.700 1.000 1 2015 2015
dbSNP: rs10114470
rs10114470
4 0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 0.010 1.000 1 2017 2017
dbSNP: rs10142466
rs10142466
1 14 68805067 intergenic variant A/C;G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs1020856343
rs1020856343
5 0.851 0.240 5 132393705 missense variant C/T snv 4.0E-06 0.020 1.000 2 2006 2010
dbSNP: rs1042058
rs1042058
2 1.000 0.040 10 30439172 synonymous variant T/C snv 0.51 0.45 0.800 1.000 2 2012 2017
dbSNP: rs1042522
rs1042522
242 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 0.010 1.000 1 2017 2017
dbSNP: rs1045642
rs1045642
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.100 0.800 10 2003 2015
dbSNP: rs10486483
rs10486483
2 1.000 0.040 7 26852821 intron variant G/A snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs104895094
rs104895094
5 0.851 0.320 16 3243403 missense variant T/A;C snv 8.0E-06; 5.2E-03 0.010 1.000 1 2013 2013
dbSNP: rs104895467
rs104895467
5 0.851 0.120 16 50716899 missense variant A/G snv 1.2E-03 7.5E-04 0.010 1.000 1 2018 2018
dbSNP: rs10491434
rs10491434
2 1.000 0.080 5 35877812 3 prime UTR variant A/G snv 0.32 0.010 1.000 1 2014 2014
dbSNP: rs1049526
rs1049526
3 0.925 0.040 6 32981027 3 prime UTR variant C/T snv 0.93 0.700 1.000 1 2016 2016
dbSNP: rs10495903
rs10495903
2 1.000 0.040 2 43579779 intron variant C/T snv 0.13 0.800 1.000 2 2012 2017
dbSNP: rs10499563
rs10499563
7 0.807 0.120 7 22720869 intron variant T/C snv 0.21 0.010 1.000 1 2016 2016
dbSNP: rs10500264
rs10500264
2 1.000 0.080 19 33259408 intergenic variant G/A snv 0.14 0.820 1.000 2 2009 2019
dbSNP: rs1050152
rs1050152
10 0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 0.040 1.000 4 2006 2017
dbSNP: rs1051792
rs1051792
5 0.851 0.240 6 31411200 missense variant G/A snv 0.34 0.35 0.010 1.000 1 2010 2010
dbSNP: rs10521318
rs10521318
1 16 85977731 intron variant C/G;T snv 0.800 1.000 1 2012 2012
dbSNP: rs10748781
rs10748781
11 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 0.700 1.000 1 2015 2015