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: rs56702977
rs56702977
1 15 42379110 intron variant G/A snv 0.16 0.700 1.000 1 2016 2016
dbSNP: rs8026198
rs8026198
1 15 42361263 intron variant A/C;T snv 0.700 1.000 1 2017 2017