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: rs1234214
rs1234214
1 10 87938433 intron variant C/A snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs3831732
rs3831732
2 10 87895485 intron variant -/A;AA delins 0.700 1.000 1 2016 2016