List of variants in gene NEXN reported by Blueprint Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_144573.4(NEXN):c.1788T>G (p.Ser596Arg)	rs199738750	0.00029
NM_144573.4(NEXN):c.835C>T (p.Arg279Cys)	rs146245480	0.00025
NM_144573.4(NEXN):c.1582G>C (p.Glu528Gln)	rs200071700	0.00011
NM_144573.4(NEXN):c.1955A>G (p.Tyr652Cys)	rs137853197	0.00010
NM_144573.4(NEXN):c.1053+1G>A	rs397517843	0.00007
NM_144573.4(NEXN):c.865-5G>A	rs727505353	0.00005
NM_144573.4(NEXN):c.1400T>C (p.Ile467Thr)	rs370195451	0.00002
NM_144573.4(NEXN):c.1112C>T (p.Pro371Leu)	rs200067011
NM_144573.4(NEXN):c.1589_1590del (p.Arg530fs)	rs869025492
NM_144573.4(NEXN):c.1630del (p.Gln544fs)	rs730880172

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