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: rs139141690
rs139141690
3 7 101856650 intron variant G/A snv 2.2E-03 0.700 1.000 1 2016 2016
dbSNP: rs412332
rs412332
1 7 102064238 intron variant C/G;T snv 0.700 1.000 1 2016 2016