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: rs6796
rs6796
3 7 6462736 3 prime UTR variant T/C snv 0.30 0.700 1.000 1 2016 2016
dbSNP: rs73057397
rs73057397
3 7 6464609 intron variant T/C snv 0.43 0.700 1.000 1 2018 2018