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: rs2276824
rs2276824
3 3 52603470 intron variant C/G snv 0.54 0.61 0.700 1.000 1 2017 2017