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: rs6700559
rs6700559
1 1.000 0.040 1 200676945 intron variant C/T snv 0.43 0.800 1.000 2 2013 2018