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: rs6903575
rs6903575
1 6 73794007 intron variant G/A snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs6909201
rs6909201
1 6 73754171 intron variant A/G snv 0.55 0.700 1.000 1 2018 2018