Variants in gene SIK1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 6

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HGVS	dbSNP	gnomAD frequency
NM_173354.5(SIK1):c.2087C>T (p.Pro696Leu)	rs56386767	0.00709
NM_173354.5(SIK1):c.1463-7C>T	rs142866662	0.00575
NM_173354.5(SIK1):c.1215G>A (p.Met405Ile)	rs34987632	0.00446
NM_173354.5(SIK1):c.1119+7G>A	rs201075575	0.00128
NM_173354.5(SIK1):c.855G>A (p.Pro285=)	rs549052367	0.00006
NM_173354.5(SIK1):c.274-3del	rs550878772

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