ClinVar Miner

Submissions for variant NM_138554.5(TLR4):c.526_544del (p.Asn176fs)

dbSNP: rs749154041
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine RCV002223166 SCV002500975 uncertain significance not specified no assertion criteria provided literature only
Al Jalila Children's Genomics Center, Al Jalila Childrens Speciality Hospital RCV003120839 SCV003798481 likely risk allele Susceptibility to severe COVID-19 2022-07-01 no assertion criteria provided research

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