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: rs7574865
rs7574865
59 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.900 1.000 11 2008 2017
dbSNP: rs706778
rs706778
19 0.695 0.320 10 6056986 intron variant C/T snv 0.46 0.810 0.750 4 2011 2019
dbSNP: rs1893217
rs1893217
14 0.742 0.440 18 12809341 intron variant A/G snv 0.12 0.810 1.000 3 2011 2019
dbSNP: rs3087456
rs3087456
14 0.742 0.480 16 10877045 intron variant G/A snv 0.53 0.030 0.667 3 2006 2012
dbSNP: rs13151961
rs13151961
7 0.827 0.200 4 122194347 intron variant A/G snv 0.11 0.710 1.000 2 2010 2011
dbSNP: rs1678542
rs1678542
9 0.790 0.320 12 57574932 intron variant C/G snv 0.42 0.710 1.000 2 2011 2015
dbSNP: rs2056626
rs2056626
5 0.882 0.080 1 167451188 intron variant T/G snv 0.30 0.710 1.000 2 2011 2013
dbSNP: rs2104286
rs2104286
25 0.662 0.440 10 6057082 intron variant T/C snv 0.18 0.020 1.000 2 2009 2015
dbSNP: rs2281808
rs2281808
4 0.925 0.160 20 1629905 intron variant T/A;C snv 0.020 1.000 2 2018 2019
dbSNP: rs2488457
rs2488457
11 0.763 0.480 1 113872746 intron variant G/A;C snv 0.020 0.500 2 2012 2013
dbSNP: rs2816316
rs2816316
5 0.882 0.200 1 192567683 intron variant C/A snv 0.79 0.710 1.000 2 2011 2017
dbSNP: rs3761548
rs3761548
42 0.620 0.680 X 49261784 intron variant G/A;T snv 0.020 1.000 2 2013 2013
dbSNP: rs4810485
rs4810485
16 0.732 0.480 20 46119308 intron variant T/A;G snv 0.710 1.000 2 2011 2016
dbSNP: rs5844572
rs5844572
11 0.752 0.360 22 23893562 intron variant -/ATTC delins 0.020 1.000 2 2017 2019
dbSNP: rs6840978
rs6840978
10 0.776 0.160 4 122633552 intron variant C/T snv 0.16 0.800 1.000 2 2011 2019
dbSNP: rs755622
rs755622
44 0.611 0.720 22 23894205 intron variant G/C snv 0.26 0.020 1.000 2 2017 2019
dbSNP: rs864537
rs864537
4 0.925 0.200 1 167442147 intron variant A/G snv 0.29 0.810 1.000 2 2011 2013
dbSNP: rs1032129
rs1032129
5 0.851 0.040 8 118939661 intron variant A/C snv 0.37 0.700 1.000 1 2019 2019
dbSNP: rs10460003
rs10460003
2 18 12747013 intron variant C/T snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs10494079
rs10494079
4 0.882 1 107832253 intron variant G/C snv 9.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs10752747
rs10752747
2 1 2593476 intron variant G/T snv 0.41 0.700 1.000 1 2011 2011
dbSNP: rs10806425
rs10806425
6 0.851 0.280 6 90216893 intron variant C/A snv 0.33 0.700 1.000 1 2011 2011
dbSNP: rs10892258
rs10892258
4 0.925 0.120 11 118709156 intron variant G/A snv 0.19 0.700 1.000 1 2011 2011
dbSNP: rs10892279
rs10892279
3 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 0.800 1.000 1 2011 2011
dbSNP: rs10892286
rs10892286
2 11 118771376 intron variant A/C snv 0.17 0.700 1.000 1 2011 2011