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: rs4733724
rs4733724
2 1.000 0.040 8 129711482 intron variant A/G snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs60890741
rs60890741
1 1.000 0.040 8 129756257 intron variant -/A;AA delins 0.700 1.000 1 2019 2019