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

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_014908.4(DOLK):c.-49A>G	rs116439010	0.01852
NM_014908.4(DOLK):c.1dup (p.Met1fs)	rs531969689	0.00573
NM_014908.4(DOLK):c.186G>A (p.Arg62=)	rs148171062	0.00299
NM_014908.4(DOLK):c.771C>T (p.Ile257=)	rs147416890	0.00205
NM_014908.4(DOLK):c.1450A>G (p.Ile484Val)	rs147630977	0.00044
NM_014908.4(DOLK):c.1437T>C (p.Ser479=)	rs574290806	0.00019
NM_014908.4(DOLK):c.1011A>G (p.Arg337=)	rs375939944	0.00005

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