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: rs339969
rs339969
2 15 60591082 intron variant C/A snv 0.68 0.800 1.000 2 2011 2018
dbSNP: rs340005
rs340005
3 15 60585831 intron variant G/A snv 0.67 0.800 1.000 2 2012 2019
dbSNP: rs2414679
rs2414679
1 15 60687613 intron variant C/G snv 0.40 0.700 1.000 1 2019 2019