List of variants in gene LOXHD1 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001384474.1(LOXHD1):c.4244G>A (p.Arg1415Gln)	rs374728484	0.00073
NM_001384474.1(LOXHD1):c.5410G>A (p.Glu1804Lys)	rs200242497	0.00056
NM_001384474.1(LOXHD1):c.1562A>G (p.Asn521Ser)	rs556312555	0.00002
NM_001384474.1(LOXHD1):c.6497C>G (p.Pro2166Arg)	rs200198786	0.00001
NM_001384474.1(LOXHD1):c.197C>T (p.Thr66Met)	rs199536893

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