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: rs41280378
rs41280378
1 10 72932888 3 prime UTR variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs57176252
rs57176252
1 10 72902835 intron variant C/A snv 4.3E-02 0.700 1.000 1 2018 2018