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: rs13083798
rs13083798
3 3 52615732 intron variant A/G snv 0.51 0.700 1.000 1 2017 2017
dbSNP: rs2590838
rs2590838
3 3 52588070 intron variant G/A snv 0.55 0.700 1.000 1 2017 2017