ClinVar Miner

Submissions for variant NM_138554.5(TLR4):c.1196C>T (p.Thr399Ile) (rs4986791)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000007043 SCV000027239 benign TLR4 POLYMORPHISM 2002-07-18 no assertion criteria provided literature only
NEI Ophthalmic Genomics Laboratory,National Institutes of Health RCV000086999 SCV000119252 not provided not provided no assertion provided not provided

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