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: rs3762988
rs3762988
3 5 32709547 5 prime UTR variant C/T snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs3828591
rs3828591
3 5 32713002 intron variant G/C snv 0.43 0.700 1.000 1 2018 2018