List of variants in gene LOXHD1 reported as likely benign by Illumina Laboratory Services, Illumina

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_001384474.1(LOXHD1):c.6183-11del	rs143514947	0.23567
NM_001384474.1(LOXHD1):c.2175C>T (p.Asn725=)	rs2086005	0.09206
NM_001384474.1(LOXHD1):c.5399+13G>A	rs59128481	0.07068
NM_001384474.1(LOXHD1):c.4868A>G (p.Glu1623Gly)	rs12606417	0.06993
NM_001384474.1(LOXHD1):c.1087G>A (p.Val363Ile)	rs10163657	0.05881
NM_001384474.1(LOXHD1):c.2T>A (p.Met1Lys)	rs36024592	0.02382
NM_001384474.1(LOXHD1):c.2370C>T (p.Asp790=)	rs34723936	0.01692
NM_001384474.1(LOXHD1):c.4148C>T (p.Thr1383Met)	rs7244681

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