List of variants in gene combination CAD, LOC126806171 reported as benign for not provided

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004341.5(CAD):c.2400+190G>C	rs73921482	0.06479
NM_004341.5(CAD):c.2646-35C>T	rs6747264	0.05810
NM_004341.5(CAD):c.2748C>T (p.Tyr916=)	rs140011289	0.00864
NM_004341.5(CAD):c.2497G>A (p.Asp833Asn)	rs115483555	0.00560
NM_004341.5(CAD):c.2577G>A (p.Pro859=)	rs147159197	0.00001
NM_004341.5(CAD):c.2401-12C>T	rs200243379
NM_004341.5(CAD):c.2646-3dup

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