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: rs9469578
rs9469578
2 6 33738702 intron variant C/T snv 0.11 0.800 1.000 1 2010 2010
dbSNP: rs73743323
rs73743323
2 6 33737578 intron variant C/T snv 0.11 0.700 1.000 1 2018 2018