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: rs16958445
rs16958445
1 1.000 0.040 15 73884216 missense variant G/A snv 3.2E-02 1.2E-02 0.810 1.000 2 2014 2019
dbSNP: rs16958415
rs16958415
1 1.000 0.040 15 73875834 intron variant G/A snv 6.4E-02 0.700 1.000 1 2014 2014
dbSNP: rs4445847
rs4445847
1 1.000 0.040 15 73879672 intron variant C/A;T snv 0.700 1.000 1 2014 2014
dbSNP: rs4886725
rs4886725
1 1.000 0.040 15 73878665 intron variant G/A snv 0.28 0.700 1.000 1 2014 2014
dbSNP: rs12914489
rs12914489
2 1.000 0.040 15 73895596 intergenic variant G/A;T snv 8.2E-02 0.010 1.000 1 2011 2011