Write a script to get gene-aggregated counts for DB columns in an annotated VCF.
Input:
- An annotated, filtered VCF file output from the script by @nicovbing that implements Issue 8
Output:
- Insert row in the "GeneUserData" table with counts for the number of variants in columns "In ClinVar", "High impact", "Missense", etc. -- one row per gene per upload
- Foreign key should be Entrez Gene ID (column named "slot", perhaps)