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: rs1000778
rs1000778
3 1.000 0.040 11 61887833 intron variant A/G snv 0.59 0.010 1.000 1 2017 2017
dbSNP: rs10033464
rs10033464
8 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 0.010 1.000 1 2017 2017
dbSNP: rs10033601
rs10033601
1 1.000 0.040 4 152330909 intron variant A/G snv 0.37 0.42 0.010 1.000 1 2017 2017
dbSNP: rs1004638
rs1004638
3 1.000 0.040 9 22115590 intron variant A/C;T snv 0.010 1.000 1 2009 2009
dbSNP: rs1007888
rs1007888
4 0.882 0.120 22 23898914 non coding transcript exon variant C/T snv 0.46 0.010 1.000 1 2016 2016
dbSNP: rs1008949
rs1008949
1 1.000 0.040 8 22696108 intron variant T/A;C;G snv 0.010 < 0.001 1 2014 2014
dbSNP: rs1010
rs1010
7 0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 0.010 1.000 1 2007 2007
dbSNP: rs10116253
rs10116253
4 0.851 0.120 9 117702042 upstream gene variant T/C snv 0.28 0.010 1.000 1 2017 2017
dbSNP: rs10116277
rs10116277
8 0.827 0.160 9 22081398 intron variant G/T snv 0.62 0.010 1.000 1 2011 2011
dbSNP: rs10159239
rs10159239
3 0.882 0.040 1 247443750 intron variant G/A snv 0.57 0.010 1.000 1 2020 2020
dbSNP: rs1018383
rs1018383
1 1.000 0.040 6 11784092 intron variant C/T snv 0.76 0.010 1.000 1 2015 2015
dbSNP: rs1020608562
rs1020608562
9 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 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 2019 2019
dbSNP: rs10401969
rs10401969
25 0.776 0.240 19 19296909 intron variant T/C snv 0.10 0.010 1.000 1 2016 2016
dbSNP: rs1041981
rs1041981
25 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 0.010 1.000 1 2011 2011
dbSNP: rs1044925
rs1044925
6 0.827 0.120 1 179354603 3 prime UTR variant C/A;G snv 0.010 1.000 1 2014 2014
dbSNP: rs1048990
rs1048990
8 0.790 0.280 14 35292469 5 prime UTR variant C/G;T snv 0.19; 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs1049255
rs1049255
9 0.776 0.320 16 88643329 3 prime UTR variant C/T snv 0.49 0.48 0.010 < 0.001 1 2017 2017
dbSNP: rs1049353
rs1049353
42 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 0.010 < 0.001 1 2012 2012
dbSNP: rs1049673
rs1049673
7 0.807 0.160 7 80677034 3 prime UTR variant C/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs1050286
rs1050286
3 0.882 0.160 12 10158964 3 prime UTR variant T/C snv 0.40 0.010 1.000 1 2016 2016
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: rs10509681
rs10509681
8 0.807 0.160 10 95038992 missense variant T/C snv 8.3E-02 8.0E-02 0.010 1.000 1 2007 2007
dbSNP: rs1051009
rs1051009
1 1.000 0.040 17 4734591 3 prime UTR variant G/A snv 0.35 0.27 0.010 1.000 1 2010 2010
dbSNP: rs1051339
rs1051339
3 0.882 0.040 10 89247582 missense variant C/T snv 9.5E-02 0.13 0.010 1.000 1 2019 2019