Variants in gene PLOD1 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: 13

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HGVS	dbSNP	gnomAD frequency
NM_000302.4(PLOD1):c.295G>A (p.Ala99Thr)	rs7551175	0.26545
NM_000302.4(PLOD1):c.358G>T (p.Ala120Ser)	rs2273285	0.14145
NM_000302.4(PLOD1):c.2124T>C (p.His708=)	rs879690	0.04545
NM_000302.4(PLOD1):c.250G>A (p.Ala84Thr)	rs34878020	0.02621
NM_000302.4(PLOD1):c.540G>A (p.Gln180=)	rs35958757	0.01887
NM_000302.4(PLOD1):c.302+15G>A	rs140227667	0.00760
NM_000302.4(PLOD1):c.1141G>A (p.Val381Met)	rs2230896	0.00668
NM_000302.4(PLOD1):c.802A>G (p.Thr268Ala)	rs74354225	0.00370
NM_000302.4(PLOD1):c.976-16C>T	rs142329815	0.00073
NM_000302.4(PLOD1):c.1756-13C>T	rs370882934	0.00038
NM_000302.4(PLOD1):c.509A>T (p.Glu170Val)	rs554232128	0.00003
NM_000302.4(PLOD1):c.1903-14dup	rs748794198
NM_000302.4(PLOD1):c.555G>T (p.Lys185Asn)	rs142978362

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