ClinVar Miner

Submissions for variant NM_001042750.2(STAG2):c.541G>A (p.Val181Met)

gnomAD frequency: 0.00015  dbSNP: rs202127296
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 RCV000935167 SCV001080908 benign not provided 2023-09-21 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000935167 SCV002063352 likely benign not provided 2021-10-01 criteria provided, single submitter clinical testing

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