ClinVar Miner

Submissions for variant NM_198994.3(TGM6):c.1968C>T (p.Asp656=)

gnomAD frequency: 0.00006  dbSNP: rs141258102
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
Invitae RCV000974659 SCV001122494 likely benign not provided 2023-10-13 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000974659 SCV001153417 uncertain significance not provided 2018-12-01 criteria provided, single submitter clinical testing

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