ClinVar Miner

Submissions for variant NM_170665.4(ATP2A2):c.2860-10TG[2]

dbSNP: rs372303998
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000359763 SCV000376251 likely benign Keratosis follicularis 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000960169 SCV001107124 benign not provided 2023-12-07 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000960169 SCV001143137 benign not provided 2019-05-30 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002259844 SCV002539145 benign Acrokeratosis verruciformis of Hopf 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000359763 SCV002539146 benign Keratosis follicularis 2021-12-05 criteria provided, single submitter clinical testing

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