ClinVar Miner

List of variants in gene NEXN reported as likely benign for Cardiovascular phenotype

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Total variants: 19
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NM_144573.3(NEXN):c.1332A>G (p.Gln444=) rs1385609119
NM_144573.3(NEXN):c.141A>G (p.Gln47=) rs1459232585
NM_144573.3(NEXN):c.1488T>C (p.Asp496=) rs754485056
NM_144573.3(NEXN):c.1704C>G (p.Gly568=) rs397517850
NM_144573.3(NEXN):c.616G>A (p.Glu206Lys) rs370428679
NM_144573.3(NEXN):c.739T>C (p.Leu247=) rs781118443
NM_144573.3(NEXN):c.78T>C (p.Leu26=) rs376535223
NM_144573.3(NEXN):c.856C>T (p.Arg286Trp) rs199917913
NM_144573.4(NEXN):c.1029G>A (p.Ala343=) rs374260457
NM_144573.4(NEXN):c.1416AAG[1] (p.Arg475del) rs794729091
NM_144573.4(NEXN):c.156C>T (p.Asp52=) rs371431782
NM_144573.4(NEXN):c.1618A>G (p.Met540Val) rs201390657
NM_144573.4(NEXN):c.1671GGA[2] (p.Glu561_Glu562del) rs397517848
NM_144573.4(NEXN):c.1785C>T (p.Asp595=) rs182998780
NM_144573.4(NEXN):c.237T>C (p.Ala79=) rs727504549
NM_144573.4(NEXN):c.512T>C (p.Ile171Thr) rs372065024
NM_144573.4(NEXN):c.732C>A (p.Pro244=) rs201171783
NM_144573.4(NEXN):c.777A>G (p.Gln259=) rs375544798
NM_144573.4(NEXN):c.893C>G (p.Thr298Arg) rs200753280

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