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: rs1982094
rs1982094
5 8 129612570 intron variant C/T snv 4.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs397731840
rs397731840
5 8 129599504 intron variant TT/-;T;TTT;TTTT;TTTTT delins 0.700 1.000 1 2016 2016