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: rs1327235
rs1327235
7 20 10988382 intron variant A/G snv 0.46 0.700 1.000 7 2011 2018
dbSNP: rs13209747
rs13209747
5 6 126794309 intron variant C/G;T snv 0.36 0.700 1.000 6 2013 2018
dbSNP: rs11953630
rs11953630
6 5 158418394 intergenic variant C/A;T snv 0.700 1.000 5 2011 2018
dbSNP: rs35444
rs35444
6 12 115114632 intergenic variant A/G snv 0.38 0.700 1.000 5 2011 2018
dbSNP: rs751984
rs751984
4 11 61510774 3 prime UTR variant T/C snv 0.16 0.700 1.000 5 2016 2018
dbSNP: rs1173771
rs1173771
9 5 32814922 regulatory region variant A/G snv 0.65 0.700 1.000 4 2011 2018
dbSNP: rs12579720
rs12579720
2 12 20020830 intron variant C/A;G;T snv 0.700 1.000 4 2015 2018
dbSNP: rs13082711
rs13082711
5 3 27496418 intergenic variant T/C snv 0.16 0.700 1.000 4 2011 2018
dbSNP: rs17080102
rs17080102
3 6 150683634 5 prime UTR variant G/C snv 8.6E-02 0.700 1.000 4 2013 2018
dbSNP: rs2004776
rs2004776
AGT
5 1 230712956 intron variant C/G;T snv 0.700 1.000 4 2017 2018
dbSNP: rs419076
rs419076
6 3 169383098 intron variant T/A;C snv 0.700 1.000 4 2011 2018
dbSNP: rs6015450
rs6015450
7 20 59176062 intron variant A/G snv 0.14 0.700 1.000 4 2011 2018
dbSNP: rs167479
rs167479
5 19 11416089 missense variant T/A;C;G snv 0.700 1.000 3 2016 2017
dbSNP: rs17030613
rs17030613
7 1 112648185 intron variant A/C snv 0.19 0.700 1.000 3 2011 2018
dbSNP: rs1887320
rs1887320
6 20 10985350 intron variant G/A snv 0.46 0.700 1.000 3 2015 2018
dbSNP: rs1902859
rs1902859
4 4 80236549 regulatory region variant T/C snv 0.27 0.700 1.000 3 2015 2019
dbSNP: rs2932538
rs2932538
4 1 112673921 intron variant A/C;G snv 0.700 1.000 3 2011 2017
dbSNP: rs35443
rs35443
5 12 115115073 intergenic variant G/C snv 0.40 0.700 1.000 3 2018 2018
dbSNP: rs4247374
rs4247374
2 19 7252745 intron variant C/T snv 9.7E-02 0.700 1.000 3 2016 2018
dbSNP: rs7599598
rs7599598
2 2 96686103 missense variant A/G;T snv 0.41 0.700 1.000 3 2017 2018
dbSNP: rs900145
rs900145
4 11 13272358 upstream gene variant C/T snv 0.62 0.700 1.000 3 2016 2018
dbSNP: rs932764
rs932764
6 10 94136183 intron variant A/G snv 0.38 0.700 1.000 3 2011 2017
dbSNP: rs10077885
rs10077885
2 5 115054424 regulatory region variant C/A snv 0.56 0.700 1.000 2 2016 2018
dbSNP: rs10184428
rs10184428
5 2 164155317 intron variant C/A;G snv 0.700 1.000 2 2018 2018
dbSNP: rs1063281
rs1063281
2 2 217804009 3 prime UTR variant C/A;T snv 0.700 1.000 2 2017 2017