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: rs314277
rs314277
6 0.925 0.080 6 104959787 intron variant A/C;G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs395962
rs395962
6 6 104949543 intron variant T/G snv 0.72 0.700 1.000 1 2018 2018