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: rs6313
rs6313
82 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 0.050 1.000 5 2003 2014
dbSNP: rs643627
rs643627
1 1.000 0.040 13 46854476 intron variant T/C snv 0.27 0.010 1.000 1 2018 2018