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: rs141007801
rs141007801
2 6 21722558 intron variant A/-;AA;AAA;AAAA delins 0.700 1.000 1 2016 2016
dbSNP: rs9466161
rs9466161
1 6 21722685 intron variant T/C snv 0.25 0.700 1.000 1 2019 2019