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: rs6547741
rs6547741
7 0.807 0.080 2 27633057 intron variant G/A snv 0.53 0.710 1.000 1 2016 2016
dbSNP: rs10462706
rs10462706
6 0.827 0.080 5 1343679 intron variant C/T snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs10851478
rs10851478
6 0.827 0.080 15 49536822 intron variant T/C snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs1229984
rs1229984
83 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 0.700 1.000 1 2016 2016
dbSNP: rs1453414
rs1453414
7 0.827 0.080 11 5807854 intron variant G/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs1800628
rs1800628
6 0.827 0.080 6 31579073 downstream gene variant G/A snv 7.3E-02 0.700 1.000 1 2016 2016
dbSNP: rs2398180
rs2398180
6 0.827 0.080 15 96319940 intron variant C/T snv 0.62 0.700 1.000 1 2016 2016
dbSNP: rs3129780
rs3129780
6 0.827 0.080 6 32679924 intergenic variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs3828805
rs3828805
12 0.752 0.160 6 32668343 5 prime UTR variant T/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs77452476
rs77452476
7 0.827 0.080 9 131087186 intron variant T/G snv 0.18 0.700 1.000 1 2016 2016
dbSNP: rs79767424
rs79767424
7 0.827 0.080 5 19108581 intron variant G/T snv 4.1E-02 0.700 1.000 1 2016 2016
dbSNP: rs8181047
rs8181047
7 0.807 0.120 9 22064466 intron variant A/G snv 0.79 0.700 1.000 1 2016 2016
dbSNP: rs928674
rs928674
6 0.827 0.080 9 131076637 intron variant A/G snv 0.16 0.700 1.000 1 2016 2016
dbSNP: rs10090787
rs10090787
3 1.000 0.080 8 120798309 intron variant C/T snv 0.34 0.010 1.000 1 2017 2017
dbSNP: rs10399805
rs10399805
7 0.851 0.240 1 203186870 upstream gene variant G/A;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1045487
rs1045487
2 1.000 0.080 2 201284973 synonymous variant G/A snv 9.5E-02 0.10 0.010 1.000 1 2017 2017
dbSNP: rs1047781
rs1047781
11 0.790 0.200 19 48703374 missense variant A/T snv 3.6E-02 1.2E-02 0.010 1.000 1 2016 2016
dbSNP: rs1047840
rs1047840
19 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 0.010 1.000 1 2009 2009
dbSNP: rs1047972
rs1047972
19 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 0.010 1.000 1 2019 2019
dbSNP: rs1048638
rs1048638
CA9
10 0.807 0.160 9 35681125 3 prime UTR variant C/A;G snv 0.010 < 0.001 1 2012 2012
dbSNP: rs1057035
rs1057035
12 0.763 0.440 14 95087805 3 prime UTR variant T/C snv 0.26 0.010 1.000 1 2012 2012
dbSNP: rs10889677
rs10889677
40 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 0.010 1.000 1 2012 2012
dbSNP: rs10900598
rs10900598
4 0.882 0.120 1 204556440 3 prime UTR variant G/C;T snv 0.38 0.010 1.000 1 2012 2012
dbSNP: rs10972727
rs10972727
4 0.882 0.200 9 36110066 synonymous variant T/A snv 0.32 0.28 0.010 < 0.001 1 2011 2011
dbSNP: rs11130760
rs11130760
2 1.000 0.080 3 60210809 intron variant G/T snv 0.12 0.010 1.000 1 2017 2017