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: rs6590474
rs6590474
1 1.000 0.040 11 99982441 intron variant A/C snv 0.71 0.010 1.000 1 2009 2009
dbSNP: rs737582
rs737582
1 1.000 0.040 11 99992669 intron variant G/A snv 0.39 0.010 1.000 1 2009 2009
dbSNP: rs7947224
rs7947224
1 1.000 0.040 11 100002678 intron variant T/C snv 0.39 0.010 1.000 1 2009 2009