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: rs4924273
rs4924273
1 1.000 0.080 15 38554537 intron variant G/C snv 0.40 0.700 1.000 1 2013 2013