List of variants in gene combination LOC129389144, PLOD2 reported by Ambry Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_182943.3(PLOD2):c.475A>T (p.Ile159Phe)	rs768122346	0.00008
NM_182943.3(PLOD2):c.406G>C (p.Val136Leu)	rs1399835378	0.00001
NM_182943.3(PLOD2):c.439G>C (p.Asp147His)	rs147440183	0.00001
NM_182943.3(PLOD2):c.421G>T (p.Asp141Tyr)
NM_182943.3(PLOD2):c.425G>A (p.Gly142Glu)
NM_182943.3(PLOD2):c.436C>A (p.Pro146Thr)
NM_182943.3(PLOD2):c.437C>A (p.Pro146Gln)	rs766267153

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