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: rs3942852
rs3942852
1 1.000 0.120 11 48093537 intron variant C/T snv 0.69 0.800 1.000 1 2012 2012