List of variants in gene OAT reported as likely benign by Natera, Inc.

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_000274.4(OAT):c.969C>T (p.Tyr323=)	rs138895801	0.00110
NM_000274.4(OAT):c.1224T>C (p.His408=)	rs201864147	0.00073
NM_000274.4(OAT):c.48C>T (p.Arg16=)	rs143526711	0.00070
NM_000274.4(OAT):c.900+9C>A	rs372834151	0.00038
NM_000274.4(OAT):c.915G>T (p.Leu305=)	rs1249516048	0.00018
NM_000274.4(OAT):c.1110C>T (p.Ala370=)	rs148325838	0.00007
NM_000274.4(OAT):c.582C>T (p.Tyr194=)	rs754489812	0.00005
NM_000274.4(OAT):c.303G>A (p.Leu101=)	rs569605240	0.00003
NM_000274.4(OAT):c.816T>C (p.Thr272=)	rs778561122	0.00002
NM_000274.4(OAT):c.352A>G (p.Asn118Asp)	rs367710098	0.00001
NM_000274.4(OAT):c.1138A>G (p.Ile380Val)	rs545710763
NM_000274.4(OAT):c.1305C>T (p.Thr435=)	rs528039246

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