ClinVar Miner

Submissions for variant NM_001172560.3(SSTR5):c.693G>A (p.Ala231=)

gnomAD frequency: 0.00237  dbSNP: rs35804776
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000879214 SCV001022230 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000879214 SCV004133618 likely benign not provided 2023-03-01 criteria provided, single submitter clinical testing SSTR5: BP4, BP7, BS2
Breakthrough Genomics, Breakthrough Genomics RCV000879214 SCV005294450 benign not provided criteria provided, single submitter not provided
PreventionGenetics, part of Exact Sciences RCV003948285 SCV004762048 benign SSTR5-related disorder 2019-10-16 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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