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: rs12190030
rs12190030
4 1.000 6 30953587 3 prime UTR variant C/T snv 0.21 0.700 1.000 1 2010 2010
dbSNP: rs12697941
rs12697941
4 1.000 6 30936937 intron variant G/A snv 0.18 0.700 1.000 1 2009 2009