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
1 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