ClinVar Miner

Submissions for variant NM_000139.5(MS4A2):c.710A>G (p.Glu237Gly)

gnomAD frequency: 0.07396 dbSNP: rs569108

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
OMIM	RCV003333726	SCV000036197	benign	RECLASSIFIED - POLYMORPHISM	2001-09-01	no assertion criteria provided	literature only

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