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

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_014908.4(DOLK):c.631C>T (p.Arg211Cys)	rs145310298	0.00238
NM_014908.4(DOLK):c.1079A>G (p.Tyr360Cys)	rs138453255	0.00111
NM_014908.4(DOLK):c.700A>G (p.Met234Val)	rs139787271	0.00102
NM_014908.4(DOLK):c.671A>T (p.Asp224Val)	rs17485436	0.00074
NM_014908.4(DOLK):c.1314C>T (p.Leu438=)	rs148118523	0.00071
NM_014908.4(DOLK):c.525T>G (p.Val175=)	rs200278288	0.00045
NM_014908.4(DOLK):c.1394G>A (p.Arg465His)	rs148930043	0.00031
NM_014908.4(DOLK):c.633C>T (p.Arg211=)	rs147647278	0.00013
NM_014908.4(DOLK):c.1446G>A (p.Ala482=)	rs201027607	0.00012
NM_014908.4(DOLK):c.192A>G (p.Leu64=)	rs563156233	0.00009
NM_014908.4(DOLK):c.210C>G (p.Val70=)	rs750368652	0.00006

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