List of variants in gene ALK reported as uncertain significance for carcinoma

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004304.5(ALK):c.3359+24G>C	rs2276550	0.26990
NM_004304.5(ALK):c.4165-6C>T	rs17007646	0.20768
NM_004304.5(ALK):c.2205-116G>A
NM_004304.5(ALK):c.3451-35TCC[3]	rs775243091
NM_004304.5(ALK):c.3744-53del	rs1669420011
NM_004304.5(ALK):c.4165-19del	rs1668958808
Single allele

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