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: rs16915196
rs16915196
1 1.000 0.040 10 60600101 intron variant A/G snv 0.12 0.700 1.000 1 2014 2014
dbSNP: rs16915231
rs16915231
1 1.000 0.040 10 60615288 intron variant G/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs1938540
rs1938540
1 1.000 0.040 10 60535056 intron variant C/T snv 8.3E-02 0.700 1.000 1 2014 2014
dbSNP: rs2154393
rs2154393
1 1.000 0.040 10 60566929 intron variant C/T snv 8.7E-02 0.700 1.000 1 2014 2014
dbSNP: rs3808943
rs3808943
2 0.925 0.040 10 60391257 intron variant C/T snv 9.7E-02 0.700 1.000 1 2014 2014
dbSNP: rs4948412
rs4948412
1 1.000 0.040 10 60386818 intron variant T/C snv 7.3E-02 0.700 1.000 1 2014 2014
dbSNP: rs4948417
rs4948417
1 1.000 0.040 10 60401860 intron variant A/G snv 9.7E-02 0.700 1.000 1 2014 2014
dbSNP: rs9633553
rs9633553
1 1.000 0.040 10 60514979 intron variant T/G snv 8.3E-02 0.700 1.000 1 2014 2014
dbSNP: rs9804190
rs9804190
5 0.882 0.040 10 60080073 intron variant C/T snv 0.30 0.070 0.857 7 2009 2018
dbSNP: rs41283526
rs41283526
2 0.925 0.040 10 60145969 splice region variant T/C snv 7.6E-03 8.2E-03 0.020 1.000 2 2016 2018
dbSNP: rs10761482
rs10761482
4 0.851 0.120 10 60325579 intron variant T/C snv 0.70 0.010 1.000 1 2016 2016
dbSNP: rs139972937
rs139972937
1 1.000 0.040 10 60072953 missense variant T/C snv 2.4E-04 3.8E-04 0.010 1.000 1 2014 2014
dbSNP: rs372922084
rs372922084
1 1.000 0.040 10 60074916 missense variant A/G snv 1.6E-05 1.4E-05 0.010 1.000 1 2018 2018