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: rs2394250
rs2394250
1 1.000 0.040 6 29975879 intron variant G/T snv 0.40 0.700 1.000 1 2013 2013