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: rs855791
rs855791
38 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 0.800 1.000 7 2010 2019
dbSNP: rs837763
rs837763
5 16 88787321 upstream gene variant C/G;T snv 0.800 1.000 5 2010 2019
dbSNP: rs7776054
rs7776054
13 6 135097778 intron variant A/G snv 0.24 0.800 1.000 4 2012 2018
dbSNP: rs1799945
rs1799945
226 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 0.800 1.000 3 2012 2018
dbSNP: rs2413450
rs2413450
6 22 37074184 intron variant T/C snv 0.61 0.800 1.000 3 2012 2017
dbSNP: rs3811444
rs3811444
12 1 247876149 missense variant C/T snv 0.31 0.26 0.800 1.000 3 2012 2018
dbSNP: rs4820268
rs4820268
14 0.851 0.160 22 37073551 missense variant G/A;C snv 0.53; 4.0E-06 0.800 1.000 3 2010 2019
dbSNP: rs6987853
rs6987853
1 8 42602307 intergenic variant T/C snv 0.69 0.800 1.000 3 2012 2019
dbSNP: rs7120391
rs7120391
2 11 5209677 downstream gene variant T/C snv 3.5E-02 0.800 1.000 3 2013 2019
dbSNP: rs7775698
rs7775698
14 1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 0.800 1.000 3 2010 2012
dbSNP: rs9924561
rs9924561
3 16 264781 intron variant G/A;T snv 2.9E-05; 6.5E-03 0.800 1.000 3 2013 2019
dbSNP: rs10445033
rs10445033
1 16 88774054 intron variant G/A snv 0.49 0.800 1.000 2 2012 2019
dbSNP: rs1050828
rs1050828
15 0.790 0.200 X 154536002 missense variant C/T snv 9.1E-03 3.6E-02 0.700 1.000 2 2013 2013
dbSNP: rs11082512
rs11082512
1 18 46139716 intergenic variant G/A;C snv 0.800 1.000 2 2012 2016
dbSNP: rs11085824
rs11085824
4 19 12890733 upstream gene variant A/G snv 0.31 0.800 1.000 2 2012 2016
dbSNP: rs1122794
rs1122794
2 16 259156 intron variant C/A snv 0.19 0.800 1.000 2 2012 2013
dbSNP: rs1175550
rs1175550
5 1 3774964 intron variant A/G snv 0.31 0.800 1.000 2 2012 2016
dbSNP: rs12490036
rs12490036
1 3 196089324 intergenic variant C/T snv 0.42 0.800 1.000 2 2012 2016
dbSNP: rs13008603
rs13008603
5 2 46128709 intron variant C/A snv 0.10 0.700 1.000 2 2012 2013
dbSNP: rs1318638
rs1318638
3 6 30160096 intron variant C/T snv 0.11 0.800 1.000 2 2012 2016
dbSNP: rs13335629
rs13335629
4 16 260381 intron variant G/A;C snv 1.1E-02 0.800 1.000 2 2013 2019
dbSNP: rs13339636
rs13339636
5 16 248589 intron variant A/G snv 3.8E-02 0.800 1.000 2 2013 2017
dbSNP: rs1541252
rs1541252
2 1 203682799 5 prime UTR variant T/A;C snv 0.800 1.000 2 2012 2013
dbSNP: rs17342717
rs17342717
8 6 25821542 intron variant C/T snv 6.1E-02 0.700 1.000 2 2010 2012
dbSNP: rs1800562
rs1800562
262 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 0.700 1.000 2 2010 2012