ClinVar Miner

Submissions for variant NM_005252.4(FOS):c.528G>C (p.Lys176Asn)

gnomAD frequency: 0.00501  dbSNP: rs138334429
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000882048 SCV001025264 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000882048 SCV004130126 likely benign not provided 2022-11-01 criteria provided, single submitter clinical testing FOS: BS2
Breakthrough Genomics, Breakthrough Genomics RCV000882048 SCV005294542 benign not provided criteria provided, single submitter not provided

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