ClinVar Miner

List of variants reported as benign for inborn disorder of ornithine metabolism by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (14):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000274.4(OAT):c.1134C>T (p.Asn378=)	rs11461	0.33660
NM_002860.4(ALDH18A1):c.1115C>A (p.Ser372Tyr)	rs3765571	0.01418

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