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: rs445
rs445
9 7 92779056 intron variant C/T snv 0.14 0.800 1.000 4 2011 2019
dbSNP: rs4328821
rs4328821
3 3 128597592 intergenic variant A/G snv 0.13 0.800 1.000 3 2011 2017
dbSNP: rs10062687
rs10062687
1 5 10624754 missense variant T/G snv 0.18 0.20 0.700 1.000 2 2016 2019
dbSNP: rs1036332
rs1036332
3 1 199043349 intron variant A/C snv 0.70 0.700 1.000 2 2016 2019
dbSNP: rs1057258
rs1057258
3 2 233206983 3 prime UTR variant C/T snv 0.30 0.700 1.000 2 2016 2019
dbSNP: rs10893844
rs10893844
2 11 128315955 regulatory region variant G/C snv 0.36 0.700 1.000 2 2016 2019
dbSNP: rs11204682
rs11204682
4 1 150623061 intron variant G/A;T snv 0.700 1.000 2 2016 2019
dbSNP: rs11555542
rs11555542
2 14 93951185 missense variant T/C snv 3.3E-02 3.7E-02 0.700 1.000 2 2016 2019
dbSNP: rs12705849
rs12705849
1 7 113142501 intron variant G/A snv 0.32 0.700 1.000 2 2016 2019
dbSNP: rs12820863
rs12820863
2 12 4209557 intergenic variant C/T snv 0.27 0.700 1.000 2 2016 2019
dbSNP: rs13089722
rs13089722
1 3 128587914 regulatory region variant G/A snv 0.11 0.700 1.000 2 2017 2019
dbSNP: rs150640087
rs150640087
2 7 50376454 intron variant G/T snv 1.0E-02 0.700 1.000 2 2016 2019
dbSNP: rs1695315
rs1695315
1 3 3111655 intron variant G/A snv 0.56 0.700 1.000 2 2016 2019
dbSNP: rs175705
rs175705
2 14 75509305 intergenic variant C/A;G;T snv 0.700 1.000 2 2016 2019
dbSNP: rs17758695
rs17758695
10 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 2 2016 2019
dbSNP: rs2075995
rs2075995
3 1 23520972 missense variant C/A snv 0.45 0.39 0.700 1.000 2 2016 2019
dbSNP: rs2296618
rs2296618
2 1 198697103 intron variant A/G snv 0.21 0.700 1.000 2 2016 2019
dbSNP: rs2579500
rs2579500
1 2 96535945 upstream gene variant G/A;C snv 0.700 1.000 2 2016 2019
dbSNP: rs34173062
rs34173062
3 8 144103704 missense variant G/A;C snv 7.3E-02 0.700 1.000 2 2016 2019
dbSNP: rs36084354
rs36084354
3 19 1079960 missense variant G/A snv 5.7E-02 5.9E-02 0.700 1.000 2 2016 2019
dbSNP: rs410867
rs410867
2 19 16316300 intron variant A/G snv 0.32 0.700 1.000 2 2016 2019
dbSNP: rs45577137
rs45577137
4 8 47739071 upstream gene variant A/G;T snv 0.700 1.000 2 2016 2019
dbSNP: rs4802399
rs4802399
2 19 38409359 3 prime UTR variant G/A snv 5.5E-02 0.700 1.000 2 2016 2019
dbSNP: rs4848100
rs4848100
2 2 111630955 non coding transcript exon variant C/T snv 0.76 0.700 1.000 2 2016 2019
dbSNP: rs511515
rs511515
2 6 33573730 3 prime UTR variant A/G snv 0.73 0.700 1.000 2 2016 2019