List of variants in gene SUN2 reported as benign for cardiovascular disorder

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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: 13

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HGVS	dbSNP	gnomAD frequency
NM_015374.3(SUN2):c.266T>G (p.Leu89Arg)	rs35496634	0.07876
NM_015374.3(SUN2):c.656C>T (p.Pro219Leu)	rs1883206	0.01037
NM_015374.3(SUN2):c.424+17C>T	rs114206377	0.00920
NM_015374.3(SUN2):c.614+6C>T	rs116680988	0.00890
NM_015374.3(SUN2):c.97A>G (p.Thr33Ala)	rs2072799	0.00592
NM_015374.3(SUN2):c.155G>A (p.Arg52His)	rs4510314	0.00486
NM_015374.3(SUN2):c.485C>T (p.Ala162Val)	rs62639696	0.00464
NM_015374.3(SUN2):c.615-19G>A	rs189559627	0.00287
NM_015374.3(SUN2):c.471C>T (p.Ser157=)	rs146940466	0.00160
NM_015374.3(SUN2):c.286+18C>T	rs202130199	0.00086
NM_015374.3(SUN2):c.614+7G>A	rs202214602	0.00071
NM_015374.3(SUN2):c.276C>T (p.Asp92=)	rs111670814	0.00068
NM_015374.3(SUN2):c.420C>T (p.Tyr140=)	rs201604103	0.00002

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