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: rs4910498
rs4910498
4 11 9743956 intron variant A/T snv 0.61 0.700 1.000 2 2018 2018
dbSNP: rs2649044
rs2649044
4 11 9742422 intron variant C/T snv 0.55 0.700 1.000 1 2018 2018