Results of a bottom-up interdisciplinary approach - COVID19 International analysis checklist -
annex:
(ACE) polymorphisms hypotheses - v5.0

Thank you to all contributors
For information - blood/loci: "In trans-ethnic meta-analyses for 15 hematological traits in 746,667 participants, including 184,535 non-EA individuals, we identified 5552 trait-variant associations, including 71 novel loci (not found in EA populations)" https://twitter.com/GLettre/status/1219075403987456011?s=19
"Haplotypesmarked as carriers contain the minor allele of rs10490770, which is in perfect LD in Eurasianpopulations with the leading risk polymorphisms. All carriers fall in a clade with the Neandertalgenomes."
(paper found thanks to @GeneticLifehack) https://twitter.com/GeneticLifehack/status/1279408919601991680
"The technology required, like being able to peer inside a single cell & see what proteins it’s making compared to its neighbours, has only evolved in the last few years. “(...) & that we’ll get there for this disease probably within the next decade.”" https://www.wired.co.uk/article/coronavirus-ace2
Some nuance / alternative prism from @nanogenomic
(SNP = Single-nucleotide polymorphism - some background info : https://en.wikipedia.org/wiki/Single-nucleotide_polymorphism) https://twitter.com/nanogenomic/status/1283688361979293696
As this thread includes the opinion of @nanogenomic - see this visual representation of SARS-COV-2 spike protein bound to ACE2 (red) with glycosylation (sugar modifications) on both proteins (video): https://twitter.com/nanogenomic/status/1278478845675360256
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