ClinVar Miner

Submissions for variant NM_003184.4(TAF2):c.1684-17C>T

dbSNP: rs118105771
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002144018 SCV002464075 benign not provided 2023-12-07 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002486965 SCV002803273 likely benign Microcephaly-thin corpus callosum-intellectual disability syndrome 2021-09-29 criteria provided, single submitter clinical testing

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