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: rs129128
rs129128
7 6 26125114 intron variant C/T snv 0.91 0.700 1.000 1 2012 2012
dbSNP: rs707896
rs707896
3 6 26116196 intron variant G/A snv 0.18 0.700 1.000 1 2012 2012