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: rs10261922
rs10261922
1 1.000 0.120 7 50414314 intergenic variant C/A;G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs1110701
rs1110701
1 1.000 0.120 7 50410929 intergenic variant A/G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs11770117
rs11770117
2 1.000 0.120 7 50406065 downstream gene variant A/T snv 0.41 0.700 1.000 1 2013 2013
dbSNP: rs12719019
rs12719019
2 1.000 0.120 7 50408441 downstream gene variant C/T snv 0.40 0.700 1.000 1 2013 2013
dbSNP: rs12748152
rs12748152
8 1.000 0.120 1 26811902 upstream gene variant C/T snv 5.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs12887958
rs12887958
1 1.000 0.120 14 23113360 downstream gene variant C/T snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs144104656
rs144104656
3 1.000 0.120 2 118661291 regulatory region variant A/G snv 1.1E-03 0.700 1.000 1 2017 2017
dbSNP: rs1569175
rs1569175
1 1.000 0.120 2 200157231 intergenic variant T/C snv 0.88 0.700 1.000 1 2009 2009
dbSNP: rs17007695
rs17007695
4 0.851 0.120 4 141788570 intergenic variant T/C snv 7.7E-02 0.700 1.000 1 2009 2009
dbSNP: rs17032980
rs17032980
3 1.000 0.120 2 67075611 intergenic variant A/G snv 0.25 0.700 1.000 1 2015 2015
dbSNP: rs17079534
rs17079534
1 1.000 0.120 3 39805581 upstream gene variant G/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs1945213
rs1945213
1 1.000 0.120 11 56408195 upstream gene variant C/G;T snv 0.800 1.000 1 2012 2012
dbSNP: rs4266962
rs4266962
1 1.000 0.120 10 22052645 intergenic variant C/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs4463516
rs4463516
3 1.000 0.120 9 32867483 intron variant G/C;T snv 0.700 1.000 1 2015 2015
dbSNP: rs4748793
rs4748793
4 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 0.700 1.000 1 2013 2013
dbSNP: rs4982729
rs4982729
1 1.000 0.120 14 23107402 upstream gene variant T/C snv 0.66 0.700 1.000 1 2013 2013
dbSNP: rs4982731
rs4982731
1 1.000 0.120 14 23116124 downstream gene variant C/T snv 0.68 0.800 1.000 1 2013 2013
dbSNP: rs6684897
rs6684897
3 1.000 0.120 1 238128048 intergenic variant C/G snv 0.83 0.700 1.000 1 2017 2017
dbSNP: rs6944602
rs6944602
2 0.925 0.120 7 50406053 downstream gene variant G/A;T snv 0.700 1.000 1 2013 2013
dbSNP: rs920590
rs920590
3 1.000 0.120 8 19793650 regulatory region variant T/C snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs1045642
rs1045642
214 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 0.030 1.000 3 2003 2012
dbSNP: rs2032582
rs2032582
97 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 0.010 1.000 1 2014 2014
dbSNP: rs2274407
rs2274407
4 0.882 0.120 13 95206781 missense variant C/A;G;T snv 9.7E-02 0.10 0.010 1.000 1 2017 2017
dbSNP: rs121913459
rs121913459
25 0.672 0.160 9 130872896 missense variant C/T snv 0.020 1.000 2 2007 2012
dbSNP: rs1057519773
rs1057519773
4 0.851 0.160 9 130872901 missense variant T/A;C;G snv 0.010 1.000 1 2014 2014