ClinVar Miner

Submissions for variant NM_017799.4(TMEM260):c.75C>T (p.Gly25=)

gnomAD frequency: 0.00054  dbSNP: rs568060358
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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 RCV000794284 SCV000933681 likely benign not provided 2023-07-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000794284 SCV005191378 uncertain significance not provided criteria provided, single submitter not provided

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