List of variants in gene CALML6 reported as benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_138705.4(CALML6):c.288A>G (p.Ala96=)	rs35971167	0.00850
NM_138705.4(CALML6):c.207C>T (p.Pro69=)	rs35804144	0.00134
NM_138705.4(CALML6):c.260G>C (p.Gly87Ala)	rs74773083

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