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: rs4896582
rs4896582
5 6 142382740 intron variant G/A snv 0.50 0.700 1.000 1 2017 2017
dbSNP: rs6570508
rs6570508
3 6 142392705 intron variant G/A snv 0.50 0.700 1.000 1 2017 2017