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: rs3733606
rs3733606
1 4 6881285 3 prime UTR variant C/T snv 0.15 0.700 1.000 1 2014 2014
dbSNP: rs6836941
rs6836941
1 4 6855551 intron variant T/C snv 0.15 0.700 1.000 1 2018 2018