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: rs2839186
rs2839186
2 1.000 0.120 21 46270154 intron variant C/T snv 0.42 0.800 1.000 2 2013 2017