List of variants in gene combination CHD3, NAA38 reported as uncertain significance for Snijders Blok-Campeau syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
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_001005271.3(CHD3):c.250C>T (p.Pro84Ser)	rs1329540442	0.00001
NM_001005271.3(CHD3):c.250C>A (p.Pro84Thr)
NM_001005271.3(CHD3):c.45G>A (p.Met15Ile)

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