ClinVar Miner

Submissions for variant NM_002029.4(FPR1):c.576T>C (p.Asn192=)

dbSNP: rs1042229
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002241361 SCV001726846 benign Gingival disorder 2024-01-31 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001824979 SCV005312199 benign not provided criteria provided, single submitter not provided
GenomeConnect, ClinGen RCV001824979 SCV002074646 not provided not provided no assertion provided phenotyping only Variant interpreted as Benign and reported on 04-27-2020 by Lab or GTR ID 500031. GenomeConnect assertions are reported exactly as they appear on the patient-provided report from the testing laboratory. GenomeConnect staff make no attempt to reinterpret the clinical significance of the variant. This variant was reported in an individual referred for clinical diagnostic genetic testing.

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