Variants in gene ALK with conflicting interpretations "uncertain significance" and "benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) 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_004304.5(ALK):c.932G>A (p.Arg311His)	rs150966028	0.00063
NM_004304.5(ALK):c.3080C>T (p.Pro1027Leu)	rs140733978	0.00054
NM_004304.5(ALK):c.310C>T (p.Pro104Ser)	rs576431612	0.00026
NM_004304.5(ALK):c.4425C>T (p.His1475=)	rs139039449	0.00003
NM_004304.5(ALK):c.1720G>C (p.Gly574Arg)	rs762358335
NM_004304.5(ALK):c.2577G>C (p.Glu859Asp)	rs61754865

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