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: rs12328675
rs12328675
2 2 164684290 3 prime UTR variant T/C snv 0.13 0.800 1.000 2 2010 2019
dbSNP: rs13389219
rs13389219
5 1.000 0.080 2 164672366 intron variant C/T snv 0.47 0.700 1.000 1 2012 2012