ClinVar Miner

Submissions for variant NM_006502.3(POLH):c.723G>A (p.Gly241=)

dbSNP: rs781009488
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Sema4, Sema4 RCV002258738 SCV002537003 likely benign Xeroderma pigmentosum 2021-08-10 criteria provided, single submitter curation
Labcorp Genetics (formerly Invitae), Labcorp RCV003679084 SCV004405571 likely benign not provided 2023-06-01 criteria provided, single submitter clinical testing

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