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: rs4761470
rs4761470
2 12 94289428 intron variant G/A snv 0.16 0.800 1.000 1 2013 2013
dbSNP: rs575315089
rs575315089
2 12 94289428 intron variant -/T delins 2.2E-03 0.700 1.000 1 2013 2013