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: rs6090041
rs6090041
1 1.000 0.080 20 64081323 intron variant G/A snv 0.64 0.010 1.000 1 2010 2010
dbSNP: rs6090043
rs6090043
1 1.000 0.080 20 64086577 5 prime UTR variant C/T snv 0.48 0.010 1.000 1 2010 2010