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: rs10283564
rs10283564
2 9 5075628 intron variant C/G snv 0.23 0.700 1.000 1 2016 2016
dbSNP: rs62541534
rs62541534
1 9 5028921 intron variant C/G snv 0.23 0.700 1.000 1 2019 2019