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: rs880315
rs880315
9 0.925 0.120 1 10736809 intron variant T/C snv 0.32 0.700 1.000 9 2011 2018
dbSNP: rs17367504
rs17367504
9 1.000 0.040 1 11802721 intron variant A/G snv 0.14 0.700 1.000 4 2017 2018
dbSNP: rs2004776
rs2004776
AGT
5 1 230712956 intron variant C/G;T snv 0.700 1.000 4 2017 2018
dbSNP: rs17030613
rs17030613
7 1 112648185 intron variant A/C snv 0.19 0.700 1.000 3 2011 2018
dbSNP: rs2932538
rs2932538
4 1 112673921 intron variant A/C;G snv 0.700 1.000 3 2011 2017
dbSNP: rs10776752
rs10776752
4 1 112501706 intron variant G/T snv 8.8E-02 0.700 1.000 2 2018 2018
dbSNP: rs12129649
rs12129649
4 1 112688881 5 prime UTR variant G/T snv 6.6E-02 0.700 1.000 2 2017 2018
dbSNP: rs12405515
rs12405515
2 1 172388301 intron variant G/A;C;T snv 0.700 1.000 2 2017 2017
dbSNP: rs3753581
rs3753581
3 1 11860132 upstream gene variant C/A;T snv 0.700 1.000 2 2018 2018
dbSNP: rs4245739
rs4245739
21 0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 0.700 1.000 2 2016 2018
dbSNP: rs72640287
rs72640287
4 1 11905735 upstream gene variant C/T snv 2.6E-02 0.700 1.000 2 2018 2018
dbSNP: rs10745332
rs10745332
3 1 112646431 intron variant G/A snv 0.77 0.700 1.000 1 2015 2015
dbSNP: rs10916082
rs10916082
1 1 227064925 intron variant A/G snv 0.30 0.700 1.000 1 2017 2017
dbSNP: rs10920250
rs10920250
1 1 201755384 intron variant G/A snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs10926991
rs10926991
1 1 243329265 intron variant A/G snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs11102916
rs11102916
2 1 115294125 intron variant C/A snv 3.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs11466111
rs11466111
1 1 115286557 missense variant C/T snv 1.0E-02 1.2E-02 0.700 1.000 1 2017 2017
dbSNP: rs12046278
rs12046278
3 1 10739520 intron variant T/C snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs12063100
rs12063100
3 1 188865413 downstream gene variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs12078697
rs12078697
1 1 116472496 intron variant G/C snv 0.32 0.700 1.000 1 2018 2018
dbSNP: rs12080886
rs12080886
2 1 243222734 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs12118370
rs12118370
3 1 112605645 intron variant A/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs12142296
rs12142296
1 1 46076007 intron variant T/G snv 9.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs1240716
rs1240716
1 1 1410616 non coding transcript exon variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs12408022
rs12408022
1 1 217545447 intron variant C/T snv 0.22 0.700 1.000 1 2017 2017