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: rs7745274
rs7745274
1 6 127188012 intron variant G/A snv 0.56 0.800 1.000 1 2013 2013
dbSNP: rs9491696
rs9491696
1 6 127131494 intron variant C/G snv 0.45 0.800 1.000 1 2010 2015