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: rs4775041
rs4775041
4 1.000 0.040 15 58382496 intron variant G/C snv 0.24 0.800 1.000 3 2008 2019