ClinVar Miner

Submissions for variant NM_001201543.2(FAM161A):c.516C>G (p.Ser172=)

dbSNP: rs767300885
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001465211 SCV001669194 likely benign not provided 2023-10-27 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279883 SCV001467019 uncertain significance Retinitis pigmentosa 28 2020-08-13 no assertion criteria provided clinical testing

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