Variants in gene DLD 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000108.5(DLD):c.439-7T>C	rs10263341	0.66181
NM_000108.5(DLD):c.249T>C (p.Val83=)	rs2228664	0.00985
NM_000108.5(DLD):c.777A>G (p.Lys259=)	rs1065762	0.00944
NM_000108.5(DLD):c.1422A>C (p.Gly474=)	rs34453495	0.00918
NM_000108.5(DLD):c.34G>A (p.Ala12Thr)	rs75077312	0.00666
NM_000108.5(DLD):c.543A>T (p.Ile181=)	rs61749952	0.00461
NM_000108.5(DLD):c.507C>T (p.Gly169=)	rs144351432	0.00241
NM_000108.5(DLD):c.826A>T (p.Thr276Ser)	rs148873419	0.00175
NM_000108.5(DLD):c.549G>A (p.Thr183=)	rs150630885	0.00012

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