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: rs4311394
rs4311394
2 1.000 0.080 5 54004832 intron variant A/G snv 0.27 0.800 1.000 1 2009 2009
dbSNP: rs6450176
rs6450176
4 5 54002195 intron variant G/A snv 0.27 0.800 1.000 1 2012 2012