ClinVar Miner

Submissions for variant NM_003376.6(VEGFA):c.-94C>G

gnomAD frequency: 0.69806  dbSNP: rs2010963
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001618210 SCV001846722 benign not provided 2021-06-19 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 27648002, 25992764, 23957473, 25328912, 22993299, 15338501, 11978667, 24205329, 23007030, 16142870, 19653005, 23353010, 10930302, 15963467)
OMIM RCV000013007 SCV000033252 risk factor Microvascular complications of diabetes, susceptibility to, 1 2002-05-01 no assertion criteria provided literature only

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