ClinVar Miner

Submissions for variant NM_000619.3(IFNG):c.115-156A>G

gnomAD frequency: 0.00038 dbSNP: rs121913163

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
Human Evolutionary Genetics, Institut Pasteur	RCV000097425	SCV000121639	not provided	not provided		no assertion provided	not provided

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