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: rs138151052
rs138151052
2 4 68484175 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs976058
rs976058
1 4 68475769 intron variant T/C snv 0.44 0.700 1.000 1 2018 2018