ClinVar Miner

Submissions for variant NM_138413.4(HOGA1):c.260G>C (p.Ser87Thr)

gnomAD frequency: 0.00001 dbSNP: rs1167209340

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
Natera, Inc.	RCV001277807	SCV001464780	uncertain significance	Primary hyperoxaluria type 3	2020-04-11	no assertion criteria provided	clinical testing

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