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: rs445
rs445
9 7 92779056 intron variant C/T snv 0.14 0.700 1.000 3 2011 2018
dbSNP: rs8179
rs8179
8 0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv 0.700 1.000 1 2016 2016