List of variants reported as likely benign for arthrogryposis multiplex congenita by Natera, Inc.

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Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_012243.3(SLC35A3):c.63T>G (p.Val21=)	rs141542767	0.00038
NM_001003722.2(GLE1):c.643-4A>G	rs369804957	0.00020
NM_012243.3(SLC35A3):c.348G>A (p.Thr116=)	rs574333514	0.00006

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