ClinVar Miner

Submissions for variant NM_014244.5(ADAMTS2):c.2933G>A (p.Arg978His)

gnomAD frequency: 0.00029  dbSNP: rs201998372
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001240352 SCV001413287 uncertain significance Ehlers-Danlos syndrome, dermatosparaxis type 2022-07-26 criteria provided, single submitter clinical testing This sequence change replaces arginine, which is basic and polar, with histidine, which is basic and polar, at codon 978 of the ADAMTS2 protein (p.Arg978His). The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This variant has not been reported in the literature in individuals affected with ADAMTS2-related conditions. ClinVar contains an entry for this variant (Variation ID: 965817). Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Benign"; Align-GVGD: "Class C0"). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.
Fulgent Genetics, Fulgent Genetics RCV001240352 SCV005671631 uncertain significance Ehlers-Danlos syndrome, dermatosparaxis type 2023-12-26 criteria provided, single submitter clinical testing

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