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: rs1347297
rs1347297
1 1.000 0.080 2 178380259 intron variant C/T snv 0.24 0.710 1.000 1 2016 2016