List of variants reported as uncertain significance for syndromic craniosynostosis by Centogene AG - the Rare Disease Company

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

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001395413.1(POR):c.1882G>A (p.Val628Ile)	rs145782750	0.00106
NM_207037.2(TCF12):c.2068C>T (p.Pro690Ser)	rs2061739586

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