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: rs3134945
rs3134945
6 0.827 0.240 6 32178715 intron variant C/A snv 0.18 0.700 1.000 1 2010 2010
dbSNP: rs3134947
rs3134947
2 0.925 0.120 6 32177428 intron variant C/T snv 0.18 0.700 1.000 1 2010 2010