SACGF / SACGF/variantgrid

gnomAD gene constraint improvements

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Python
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Description

Moved to v4 and added all fields with #361 - will do this as non-critical for VG4 so separate issue:

We should write to medical scientists to get their opinion on what they want used [out of fields](https://storage.googleapis.com/gcp-public-data--gnomad/release/v4.0/constraint/README.txt)

New columns?
Perhaps EKeys for Synonymous, Missense summaries? Choose based on variant type or just populate all?

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