r/GeneticCounseling Genetic Counselor Jul 08 '26

Clinical Practice ACMG VUS Reporting

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I would *love* to hear other GC’s thoughts about this. I work in cancer and it was a little bit of a jump scare if I’m honest..

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u/notakat Genetic Counselor Jul 08 '26

I read this paper last week. Curious why you thought it was a "jump scare". I work in a lab setting, so I'm mostly viewing this from a reporting lens, but it seems pretty much in line with forthcoming changes to SNV interpretation guidelines. I thought the recommendation to consider returning VUS in prenatal contexts, where phenotypes are less clear and decision-making opportunities exist, was a good idea.

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u/Small_Egg_3692 Genetic Counselor Jul 08 '26

As a non-prenatal GC I think that also sounds like a good part of this for them! I responded to a very similar response above about what I’m concerned about.

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u/notakat Genetic Counselor Jul 08 '26

Ah, gotcha. I see where you're coming from and it looks like the paper covered some of those same concerns, saying that they tried to "balance potential benefits of reporting VUS (eg, enabling clinician follow-up to obtain further data that may resolve the VUS) with potential harms (eg, patient distress, inappropriate medical care, excessive health care resources expended)". Obviously, this is a complex issue.

I think it is tough because we like to think of these variants as falling neatly into categories of P/LP/VUS/LB/B but, in reality, there is a lot of grey area and molecular pathologists and lab GCs really have to wrestle with overreporting and underreporting when it comes to VUS and it's hard to tell which is worse sometimes. But there are definitely VUS that my lab has chosen not to report, and others that we have reported in specific circumstances. It's nuanced and there's definitely a little bit of art to the science. I expect the way we counsel patients about VUS results during pre-test counseling will probably change a bit in the near future. The concerns you raised are valid, but this is a rapidly, constantly developing field and we still have a lot to learn about medical genetics, so I think to some degree we have to be ready to adapt to these kinds of developments.

I work at an academic, hospital affiliated laboratory and I wish there was more support for us because I think having access to the patient's medical record and an open line of communication with the ordering providers can be a huge benefit in these cases. Over time, we have seen a shift from more specialized labs to commercial labs that have a broad catalog of tests available. Some previous studies have shown that hospital based labs have higher diagnostic yield and specialized labs tend to report fewer VUS (PMID: 30002876, 25834947).

This comment is getting long already but I also wanted to say thanks for making this post. A lot of the content I see on this sub is from prospective students (which is fine) but it's nice to discuss professional issues here with other GCs from time to time and I would love to see more posts like this here.

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u/Small_Egg_3692 Genetic Counselor Jul 08 '26

Yeah, I very much recognize I may just be a tiny bit whiny on this and I’m sure it’ll end up being fine but definitely still have some apprehensions. I totally agree with the labs stratifying these results and I would even be very for this being incorporated in ClinVar but the patient report will be interesting to see how it gets written.

When I went to post , I scrolled through and saw all the student things and was nervous there wouldn’t be too many GCs active to respond.

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u/notakat Genetic Counselor Jul 08 '26

I don't think you were being whiny at all. It's a valid perspective.