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: rs13102822
rs13102822
1 4 15386753 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs6449133
rs6449133
1 4 15378653 intron variant T/G snv 0.48 0.700 1.000 1 2018 2018