ClinVar Miner

List of variants reported as likely benign by Laboratory of Functional Genomics, Research Centre for Medical Genetics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_018972.4(GDAP1):c.310+6del	rs780828430	0.00109
NM_000530.8(MPZ):c.449-9C>T	rs750530042	0.00002
NM_001271.4(CHD2):c.-486T>C
NM_133433.4(NIPBL):c.8101A>G (p.Met2701Val)

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