ClinVar Miner

Submissions for variant NM_020335.3(VANGL2):c.1137A>G (p.Lys379=)

gnomAD frequency: 0.58424  dbSNP: rs12086448
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV002245205 SCV002514424 benign Neural tube defect 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004715628 SCV005283531 benign not provided criteria provided, single submitter not provided

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