List of variants in gene CA2 reported as benign for autosomal recessive osteopetrosis

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000067.3(CA2):c.663+82A>C	rs6605618	0.88940
NM_000067.3(CA2):c.562T>C (p.Leu188=)	rs703	0.64073
NM_000067.3(CA2):c.754A>G (p.Asn252Asp)	rs2228063	0.02817
NM_000067.3(CA2):c.*212A>G	rs73263450	0.02796
NM_000067.3(CA2):c.*303C>T	rs150089617	0.00878

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