List of variants in gene combination CALM1, LOC130056272 reported as likely benign for long QT syndrome

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_006888.6(CALM1):c.3+13T>C	rs745827400	0.00012
NM_006888.6(CALM1):c.3+10G>C
NM_006888.6(CALM1):c.3+14G>T

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