Realized I should have done this for @jsstevenson from the start. Some things to note:
- Clinical Significance Statements used? Diagnostic only
- What kind of variants are the Alleles? First tries transcript, then genomic
- Is the original data hgvs expressions? Like they have a few hgvs expressions and you just try one until it works, then use that for the allele expressions field?
Realized I should have done this for @jsstevenson from the start. Some things to note: