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: rs10006235
rs10006235
2 1.000 0.040 4 129748953 non coding transcript exon variant T/C snv 0.73 0.700 1.000 1 2019 2019
dbSNP: rs1000731
rs1000731
1 1.000 0.040 1 231827745 intron variant C/T snv 0.23 0.010 < 0.001 1 2018 2018
dbSNP: rs10012947
rs10012947
1 1.000 0.040 4 30491805 regulatory region variant C/T snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs10014145
rs10014145
1 1.000 0.040 4 102279420 intron variant A/G snv 0.31 0.010 1.000 1 2019 2019
dbSNP: rs10014424
rs10014424
1 1.000 0.040 4 99943207 intron variant G/A snv 6.2E-02 0.010 1.000 1 2015 2015
dbSNP: rs1001684
rs1001684
1 1.000 0.040 5 40810324 intergenic variant C/A snv 0.29 0.700 1.000 1 2011 2011
dbSNP: rs1002424
rs1002424
1 1.000 0.040 5 40767295 intron variant A/G snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs10036665
rs10036665
1 1.000 0.040 5 138252460 3 prime UTR variant T/A snv 0.16 0.010 1.000 1 2010 2010
dbSNP: rs10042486
rs10042486
4 0.882 0.040 5 63965502 intron variant C/T snv 0.58 0.020 1.000 2 2012 2016
dbSNP: rs10043986
rs10043986
2 0.925 0.040 5 79799594 missense variant C/T snv 8.7E-02 8.2E-02 0.020 1.000 2 2011 2019
dbSNP: rs10046055
rs10046055
1 1.000 0.040 5 157890009 regulatory region variant T/A snv 0.32 0.010 < 0.001 1 2006 2006
dbSNP: rs10046758
rs10046758
1 1.000 0.040 8 4326648 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10061788
rs10061788
2 1.000 0.040 5 88638889 intron variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs10063995
rs10063995
1 1.000 0.040 5 175445201 upstream gene variant G/C;T snv 0.010 1.000 1 2011 2011
dbSNP: rs10065570
rs10065570
1 1.000 0.040 5 40835525 upstream gene variant C/T snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs1006737
rs1006737
27 0.695 0.120 12 2236129 intron variant G/A snv 0.36 0.900 1.000 28 2010 2019
dbSNP: rs10074991
rs10074991
7 0.851 0.120 5 40790449 intron variant G/A snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs10077591
rs10077591
1 1.000 0.040 5 165935005 intergenic variant C/T snv 0.44 0.700 1.000 1 2017 2017
dbSNP: rs10078551
rs10078551
1 1.000 0.040 5 148621907 intron variant T/C snv 0.26 0.010 1.000 1 2010 2010
dbSNP: rs1008078
rs1008078
2 1.000 0.040 1 90724174 non coding transcript exon variant C/T snv 0.33 0.700 1.000 1 2019 2019
dbSNP: rs10082463
rs10082463
1 1.000 0.040 10 117261896 intron variant A/C;G snv 0.010 1.000 1 2013 2013
dbSNP: rs10083370
rs10083370
1 1.000 0.040 14 103847845 intron variant G/A snv 0.55 0.700 1.000 1 2018 2018
dbSNP: rs10085567
rs10085567
1 1.000 0.040 7 76104888 intron variant A/C snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs1009153
rs1009153
1 1.000 0.040 15 22896157 intron variant C/G;T snv 0.010 1.000 1 2013 2013
dbSNP: rs1009382
rs1009382
1 1.000 0.040 6 32058330 missense variant C/A;G;T snv 0.72 0.010 1.000 1 2007 2007