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: rs999845
rs999845
1 1.000 0.040 10 58776160 intron variant T/A;C snv 0.700 1.000 2 2010 2012
dbSNP: rs1002656
rs1002656
1 1.000 0.040 1 36727140 intergenic variant C/T snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs10034164
rs10034164
1 1.000 0.040 4 52593565 3 prime UTR variant A/G snv 0.18 0.010 1.000 1 2011 2011
dbSNP: rs10035449
rs10035449
1 1.000 0.040 5 165059061 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10061069
rs10061069
1 1.000 0.040 5 93735924 3 prime UTR variant G/C snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs10061623
rs10061623
1 1.000 0.040 5 135445391 3 prime UTR variant G/A;C snv 0.010 1.000 1 2013 2013
dbSNP: rs10065906
rs10065906
1 1.000 0.040 5 159580770 intron variant C/A snv 0.74 0.800 1.000 1 2013 2013
dbSNP: rs1008042
rs1008042
1 1.000 0.040 10 4583381 intergenic variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs1011633
rs1011633
1 1.000 0.040 2 99478337 intron variant C/T snv 0.43 0.700 1.000 1 2013 2013
dbSNP: rs10127497
rs10127497
1 1.000 0.040 1 66584461 intron variant A/T snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs10148293
rs10148293
1 1.000 0.040 14 74830128 intron variant A/G;T snv 0.48 0.700 1.000 1 2018 2018
dbSNP: rs1014969
rs1014969
1 1.000 0.040 3 52774325 upstream gene variant G/A snv 0.44 0.700 1.000 1 2013 2013
dbSNP: rs10175979
rs10175979
1 1.000 0.040 2 57586038 intergenic variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs10274968
rs10274968
1 1.000 0.040 7 38899654 intron variant C/T snv 0.65 0.700 1.000 1 2018 2018
dbSNP: rs1039197
rs1039197
1 1.000 0.040 10 4617005 intergenic variant A/C snv 0.71 0.700 1.000 1 2017 2017
dbSNP: rs10447426
rs10447426
DDO
1 1.000 0.040 6 110400547 intron variant G/A snv 3.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs1045430
rs1045430
1 1.000 0.040 14 74663532 3 prime UTR variant T/G snv 0.38 0.700 1.000 1 2019 2019
dbSNP: rs10457592
rs10457592
1 1.000 0.040 6 99104094 intergenic variant G/A;T snv 0.010 1.000 1 2018 2018
dbSNP: rs1048220
rs1048220
1 1.000 0.040 11 27658191 missense variant C/A snv 0.010 1.000 1 2019 2019
dbSNP: rs10484358
rs10484358
1 1.000 0.040 6 16255812 intron variant G/T snv 7.6E-02 0.800 1.000 1 2013 2013
dbSNP: rs10494994
rs10494994
1 1.000 0.040 1 215188864 intron variant G/A snv 0.17 0.010 1.000 1 2009 2009
dbSNP: rs10501696
rs10501696
1 1.000 0.040 11 89014994 intron variant A/G snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs10508287
rs10508287
1 1.000 0.040 10 4658776 intron variant A/G snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs10508288
rs10508288
1 1.000 0.040 10 4738837 intergenic variant A/G snv 0.32 0.700 1.000 1 2017 2017
dbSNP: rs10508290
rs10508290
1 1.000 0.040 10 4763511 intron variant G/A snv 9.2E-02 0.700 1.000 1 2017 2017