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: rs7843479
rs7843479
1 8 21963302 intron variant C/A;T snv 0.700 1.000 2 2010 2017
dbSNP: rs58141407
rs58141407
3 8 21934261 intron variant C/T snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs80207740
rs80207740
2 8 21922426 intron variant C/G snv 0.12 0.700 1.000 1 2018 2018