List of variants in gene COBL reported as benign for not provided

Minimum submission review status:		Collection method:
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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_015198.5(COBL):c.1801C>T (p.His601Tyr)	rs61737866	0.02562
NM_015198.5(COBL):c.141G>A (p.Ser47=)	rs115321263	0.01374
NM_015198.5(COBL):c.666C>T (p.Tyr222=)	rs76440598	0.01218
NM_015198.5(COBL):c.1963G>C (p.Ala655Pro)	rs112568753	0.01196
NM_015198.5(COBL):c.1538C>T (p.Ser513Phe)	rs61739178	0.00796
NM_015198.5(COBL):c.3702C>T (p.Thr1234=)	rs76685455	0.00432
NM_015198.5(COBL):c.171G>A (p.Ala57=)	rs79885281	0.00334

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