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: rs6431731
rs6431731
4 1.000 0.080 2 15722878 intron variant C/T snv 0.97 0.700 1.000 1 2016 2016