List of variants in gene combination CHD3, LOC126862484 reported as uncertain significance for Snijders Blok-Campeau syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001005273.3(CHD3):c.1282G>A (p.Val428Ile)	rs141138068	0.00002
NM_001005273.3(CHD3):c.1076-14G>A
NM_001005273.3(CHD3):c.1123G>A (p.Glu375Lys)	rs2151508314
NM_001005273.3(CHD3):c.1235G>A (p.Arg412Gln)

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