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: rs731839
rs731839
5 19 33408159 intron variant G/A snv 0.63 0.700 1.000 1 2012 2012
dbSNP: rs8182584
rs8182584
3 19 33418804 intron variant T/C;G snv 0.700 1.000 1 2012 2012