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: rs1353248
rs1353248
2 0.925 0.120 3 159905770 intron variant C/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs2914119
rs2914119
1 1.000 0.040 3 160026651 non coding transcript exon variant C/G;T snv 0.73 0.700 1.000 1 2019 2019
dbSNP: rs4680564
rs4680564
1 1.000 0.040 3 160146189 intron variant A/G snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs668998
rs668998
2 0.925 0.120 3 159997764 non coding transcript exon variant G/A snv 0.63 0.700 1.000 1 2019 2019
dbSNP: rs6805758
rs6805758
1 1.000 0.040 3 159927882 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs73170558
rs73170558
1 1.000 0.040 3 159973737 intron variant C/T snv 9.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs7645203
rs7645203
1 1.000 0.040 3 159968881 intron variant C/T snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs76830965
rs76830965
3 0.925 0.120 3 159919889 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019