ClinVar Miner

List of variants in gene NEXN reported as benign for Dilated cardiomyopathy 1CC; Familial hypertrophic cardiomyopathy 20

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Total variants: 11
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HGVS dbSNP
NM_144573.3(NEXN):c.1408G>C (p.Glu470Gln) rs35366555
NM_144573.3(NEXN):c.156C>T (p.Asp52=) rs371431782
NM_144573.3(NEXN):c.1618A>G (p.Met540Val) rs201390657
NM_144573.3(NEXN):c.1785C>T (p.Asp595=) rs182998780
NM_144573.3(NEXN):c.363G>A (p.Thr121=) rs35117963
NM_144573.3(NEXN):c.512T>C (p.Ile171Thr) rs372065024
NM_144573.3(NEXN):c.732C>A (p.Pro244=) rs201171783
NM_144573.3(NEXN):c.777A>G (p.Gln259=) rs375544798
NM_144573.3(NEXN):c.78T>C (p.Leu26=) rs376535223
NM_144573.3(NEXN):c.835C>T (p.Arg279Cys) rs146245480
NM_144573.3(NEXN):c.995A>C (p.Glu332Ala) rs201763096

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