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: rs2881854
rs2881854
2 4 110422107 intron variant C/A snv 0.83 0.700 1.000 1 2018 2018
dbSNP: rs6825911
rs6825911
3 4 110460482 intron variant C/T snv 0.68 0.700 1.000 1 2011 2011