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: rs3917914
rs3917914
5 1 36482287 intron variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs3917932
rs3917932
5 1 36478315 intron variant C/G snv 0.59 0.700 1.000 1 2016 2016