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: rs12202017
rs12202017
1 1.000 0.040 6 133852013 intron variant A/C;G snv 0.30 0.700 1.000 2 2015 2017
dbSNP: rs1966248
rs1966248
1 1.000 0.040 6 133838484 intron variant A/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs9493740
rs9493740
1 1.000 0.040 6 133839756 intron variant G/T snv 8.7E-02 0.700 1.000 1 2018 2018