ClinVar Miner

Submissions for variant NM_138554.5(TLR4):c.842G>A (p.Cys281Tyr)

gnomAD frequency: 0.00232  dbSNP: rs137853920
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
NEI Ophthalmic Genomics Laboratory, National Institutes of Health RCV000087000 SCV000119253 not provided not provided no assertion provided not provided

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