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: rs10983238
rs10983238
1 1.000 0.040 9 116571404 intron variant C/A;G snv 0.16 0.800 1.000 1 2008 2008
dbSNP: rs12376789
rs12376789
1 1.000 0.040 9 116620855 intron variant C/G snv 0.11 0.010 1.000 1 2016 2016