List of variants in gene SUV39H1 reported as uncertain significance for not specified

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_003173.4(SUV39H1):c.296G>A (p.Arg99Gln)	rs782344481	0.00003
NM_003173.4(SUV39H1):c.875G>A (p.Arg292His)	rs1557010122	0.00003
NM_003173.4(SUV39H1):c.298C>G (p.Arg100Gly)	rs782020916	0.00001
NM_003173.4(SUV39H1):c.1190G>A (p.Arg397His)
NM_003173.4(SUV39H1):c.402G>C (p.Glu134Asp)
NM_003173.4(SUV39H1):c.813G>A (p.Met271Ile)
NM_003173.4(SUV39H1):c.91C>A (p.Pro31Thr)

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