ClinVar Miner

List of variants in gene NEXN reported as benign by GeneDx

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Gene type:
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Total variants: 23
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HGVS dbSNP
NM_144573.3(NEXN):c.-34C>A rs758434911
NM_144573.3(NEXN):c.-52-16T>C rs557864364
NM_144573.3(NEXN):c.-58T>C rs587781100
NM_144573.3(NEXN):c.1029G>A (p.Ala343=) rs374260457
NM_144573.3(NEXN):c.1053+128T>C
NM_144573.3(NEXN):c.1251+43C>G
NM_144573.3(NEXN):c.1251+48T>C
NM_144573.3(NEXN):c.1252-301T>C
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.1659+18C>G rs147422621
NM_144573.3(NEXN):c.219+25G>A
NM_144573.3(NEXN):c.27+200T>C
NM_144573.3(NEXN):c.27+220A>C
NM_144573.3(NEXN):c.363G>A (p.Thr121=) rs35117963
NM_144573.3(NEXN):c.687+20delT rs141957231
NM_144573.3(NEXN):c.732C>A (p.Pro244=) rs201171783
NM_144573.3(NEXN):c.733G>A (p.Gly245Arg) rs1166698
NM_144573.3(NEXN):c.777A>G (p.Gln259=) rs375544798
NM_144573.3(NEXN):c.864+12T>A rs188416492
NM_144573.3(NEXN):c.864+290C>T
NM_144573.3(NEXN):c.864+294A>G
NM_144573.3(NEXN):c.995A>C (p.Glu332Ala) rs201763096

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