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: rs2067663
rs2067663
3 5 88895818 intron variant C/T snv 0.22 0.700 1.000 2 2016 2019
dbSNP: rs34367533
rs34367533
1 5 89188503 intron variant T/C;G snv 0.700 1.000 1 2019 2019