List of variants in gene NEXN reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_144573.4(NEXN):c.219+25G>A	rs1749913	0.80761
NM_144573.4(NEXN):c.864+290C>T	rs1166699	0.70342
NM_144573.4(NEXN):c.1251+43C>G	rs4483454	0.70295
NM_144573.4(NEXN):c.733G>A (p.Gly245Arg)	rs1166698	0.15380
NM_144573.4(NEXN):c.*22C>G	rs3767028	0.10567
NM_144573.4(NEXN):c.1251+48T>C	rs41312654	0.09791
NM_144573.4(NEXN):c.1474-198dup	rs150690072	0.09787
NM_144573.4(NEXN):c.1252-301T>C	rs17101082	0.08559
NM_144573.4(NEXN):c.864+294A>G	rs115465149	0.04791
NM_144573.4(NEXN):c.27+220A>C	rs74092331	0.04619
NM_144573.4(NEXN):c.489+207C>T	rs41305872	0.04062
NM_144573.4(NEXN):c.489+106T>C	rs76684082	0.02873
NM_144573.4(NEXN):c.1053+128T>C	rs74092336	0.01854
NM_144573.4(NEXN):c.27+200T>C	rs115693312	0.01669
NM_144573.4(NEXN):c.1408G>C (p.Glu470Gln)	rs35366555	0.00302
NM_144573.4(NEXN):c.995A>C (p.Glu332Ala)	rs201763096	0.00262
NM_144573.4(NEXN):c.1659+18C>G	rs147422621	0.00228
NM_144573.4(NEXN):c.864+12T>A	rs188416492	0.00141
NM_144573.4(NEXN):c.156C>T (p.Asp52=)	rs371431782	0.00128
NM_144573.4(NEXN):c.777A>G (p.Gln259=)	rs375544798	0.00077
NM_144573.4(NEXN):c.-52-16T>C	rs557864364	0.00047
NM_144573.4(NEXN):c.732C>A (p.Pro244=)	rs201171783	0.00045
NM_144573.4(NEXN):c.-58T>C	rs587781100	0.00030
NM_144573.4(NEXN):c.1029G>A (p.Ala343=)	rs374260457	0.00023
NM_144573.4(NEXN):c.865-17A>G	rs201771600	0.00016
NM_144573.4(NEXN):c.-34C>A	rs758434911
NM_144573.4(NEXN):c.1660-80del	rs374889046
NM_144573.4(NEXN):c.28-85del	rs112597766
NM_144573.4(NEXN):c.687+23del	rs141957231

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