List of variants in gene CALM1 reported as uncertain significance 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: 11

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HGVS	dbSNP	gnomAD frequency
NC_000014.8:g.(?_90863575)_(90871061_?)del
NC_000014.8:g.(?_90863575)_(90871061_?)dup
NC_000014.8:g.(?_90870713)_(90871071_?)dup
NM_006888.6(CALM1):c.106G>C (p.Val36Leu)	rs1887015236
NM_006888.6(CALM1):c.157A>G (p.Ile53Val)	rs1555365887
NM_006888.6(CALM1):c.280G>C (p.Asp94His)	rs1887099943
NM_006888.6(CALM1):c.301A>G (p.Ile101Val)	rs1595102592
NM_006888.6(CALM1):c.328A>C (p.Met110Leu)	rs2139771638
NM_006888.6(CALM1):c.4-3T>C
NM_006888.6(CALM1):c.70G>A (p.Gly24Ser)
NM_006888.6(CALM1):c.78C>T (p.Gly26=)	rs1555365884

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