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: rs3102460
rs3102460
1 1.000 0.040 1 244413415 intron variant C/T snv 0.72 0.010 1.000 1 2008 2008