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: rs1003346
rs1003346
2 1.000 9 109053060 intron variant C/A snv 0.43 0.010 1.000 1 2013 2013
dbSNP: rs10033464
rs10033464
8 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.010 1.000 1 2013 2013
dbSNP: rs10089084
rs10089084
1 8 39912430 intron variant G/C snv 0.30 0.010 1.000 1 2019 2019
dbSNP: rs1010
rs1010
7 0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 0.010 1.000 1 2009 2009
dbSNP: rs10118757
rs10118757
7 0.827 0.120 9 21853340 intron variant A/G snv 0.26 0.010 1.000 1 2009 2009
dbSNP: rs1041740
rs1041740
8 0.807 0.320 21 31667849 intron variant C/T snv 0.24 0.010 1.000 1 2012 2012
dbSNP: rs10423928
rs10423928
12 0.807 0.200 19 45679046 intron variant T/A snv 0.19 0.010 1.000 1 2016 2016
dbSNP: rs1042579
rs1042579
16 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 0.010 1.000 1 2004 2004
dbSNP: rs1042713
rs1042713
63 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 0.010 1.000 1 2011 2011
dbSNP: rs10432782
rs10432782
7 0.807 0.160 21 31664078 intron variant T/G snv 0.19 0.010 1.000 1 2012 2012
dbSNP: rs10435816
rs10435816
2 1.000 0.080 9 6225535 intron variant A/G snv 0.35 0.010 1.000 1 2019 2019
dbSNP: rs1043994
rs1043994
7 0.827 0.120 19 15192033 synonymous variant T/A;C snv 4.0E-06; 0.85 0.010 1.000 1 2015 2015
dbSNP: rs1044498
rs1044498
15 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 0.010 1.000 1 2013 2013
dbSNP: rs10478723
rs10478723
1 6 12295228 intron variant G/A snv 0.15 0.010 1.000 1 2009 2009
dbSNP: rs1048661
rs1048661
14 0.732 0.320 15 73927205 missense variant G/T snv 0.33 0.28 0.010 1.000 1 2011 2011
dbSNP: rs10488682
rs10488682
2 1.000 0.160 11 18040935 5 prime UTR variant T/A snv 0.19 0.010 1.000 1 2019 2019
dbSNP: rs104895564
rs104895564
3 0.925 0.200 19 53810809 stop gained G/A snv 1.5E-04 4.3E-04 0.010 1.000 1 2018 2018
dbSNP: rs1050450
rs1050450
43 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 0.010 1.000 1 2012 2012
dbSNP: rs10507875
rs10507875
3 0.925 0.160 13 77943119 intron variant A/G snv 0.17 0.010 1.000 1 2009 2009
dbSNP: rs1051931
rs1051931
19 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 0.010 1.000 1 2014 2014
dbSNP: rs1052700
rs1052700
3 1.000 0.040 15 89665079 3 prime UTR variant A/T snv 0.26 0.010 1.000 1 2008 2008
dbSNP: rs1057910
rs1057910
12 0.776 0.280 10 94981296 missense variant A/C;G snv 6.3E-02; 4.0E-06 0.010 1.000 1 2014 2014
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: rs10757274
rs10757274
22 0.701 0.320 9 22096056 intron variant A/G snv 0.41 0.010 1.000 1 2009 2009
dbSNP: rs10848683
rs10848683
1 12 2681964 missense variant C/T snv 4.0E-06; 0.78 0.71 0.010 1.000 1 2018 2018