List of variants in gene NLGN3 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_181303.2(NLGN3):c.1954A>G (p.Thr652Ala)	rs144914894	0.00197
NM_181303.2(NLGN3):c.807C>T (p.Ser269=)	rs151276700	0.00064
NM_181303.2(NLGN3):c.1113C>T (p.His371=)	rs374424855	0.00012
NM_181303.2(NLGN3):c.435C>T (p.Asn145=)	rs771275997	0.00011
NM_181303.2(NLGN3):c.2064C>T (p.Asn688=)	rs368751962	0.00003
NC_000023.11:g.71171625C>T
NC_000023.11:g.71171667G>A
NM_181303.2(NLGN3):c.2331C>T (p.Ala777=)	rs759656254

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