List of variants in gene PLOD3 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001084.5(PLOD3):c.1144G>C (p.Asp382His)	rs41281013	0.00583
NM_001084.5(PLOD3):c.1797G>A (p.Arg599=)	rs139049819	0.00393
NM_001084.5(PLOD3):c.535A>G (p.Ile179Val)	rs34646598	0.00305
NM_001084.5(PLOD3):c.1678G>C (p.Glu560Gln)	rs140879834	0.00078
NM_001084.5(PLOD3):c.1614C>T (p.Val538=)	rs148949172	0.00033
NM_001084.5(PLOD3):c.477G>A (p.Thr159=)	rs201433094	0.00006
NM_001084.5(PLOD3):c.812A>G (p.Asn271Ser)	rs535949022	0.00003
NM_001084.5(PLOD3):c.1992G>A (p.Leu664=)

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