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Looks like that's it: "We identified 2 coding variants: one rare variant which was observed in a single control (c.401G>A; p.S134N) and one common variant (rs3173615, pT185S)." (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3034409/)

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Heads-up: 23andme data contains this gene:

cmbpr:raw_23andme caleb$ grep rs1990622 *.txt

genome_Person1.txt:rs1990622 7 12283787 GG

genome_Person2.txt:rs1990622 7 12283787 GG

genome_Person3.txt:rs1990622 7 12283787 AG

I have 'A or G'

https://itsosticky.com/1qz58aj

Any idea what this means?

I hope someone who understands the article can offer an explanation about whether it's possible to use the 23andme data to speculate about one's own susceptibility to this.

Seconded.

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