ClinVar Miner

Submissions for variant NM_001388492.1(HTT):c.9213G>A (p.Ala3071=)

gnomAD frequency: 0.00003  dbSNP: rs369633799
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002189362 SCV002344912 likely benign not provided 2022-08-16 criteria provided, single submitter clinical testing

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