ClinVar Miner

Submissions for variant NM_000369.5(TSHR):c.1783G>A (p.Val595Ile)

gnomAD frequency: 0.00077  dbSNP: rs142632518
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 RCV000878919 SCV001021910 likely benign not provided 2024-02-23 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000878919 SCV004236985 uncertain significance not provided 2023-06-29 criteria provided, single submitter clinical testing

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