GET-Evidence Report huA38896 (WGC069900D.vcf.gz)

Likely Pathogenic and Rare (<2.5% Allele Freq.)
All
Insufficiently evaluated variants

Variant	Clinical Importance	Impact	Zygosity	Ref. Allele	Alt. Allele(s)	Allele Freq.	Summary

Variant	Clinical Importance	Impact	Zygosity	Ref. Allele	Alt. Allele(s)	Allele Freq.	Summary

Variant	Prioritization	Allele Freq.	Num. of articles	Zygosity	Prioritization Reasons