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: rs9966612
rs9966612
1 1.000 0.120 18 649311 intron variant A/C;G snv 0.700 1.000 1 2017 2017