ClinVar Miner

Submissions for variant NM_000029.4(AGT):c.803T>C (p.Met268Thr) (rs699)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000242838 SCV000301563 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000405686 SCV000355399 benign Renal dysplasia 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV000835695 SCV000977501 benign not provided 2018-03-13 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
OMIM RCV000019691 SCV000039989 risk factor Hypertension, essential, susceptibility to 2005-01-01 no assertion criteria provided literature only
OMIM RCV000019692 SCV000039990 risk factor Preeclampsia, susceptibility to 2005-01-01 no assertion criteria provided literature only
OMIM RCV000019693 SCV000039991 risk factor Susceptibility to progression to renal failure in IgA nephropathy 2005-01-01 no assertion criteria provided literature only

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