List of variants in gene NLGN4X reported as benign by Eurofins NTD LLC (GA)

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_181332.3(NLGN4X):c.933C>T (p.Thr311=)	rs7049300	0.13090
NM_181332.3(NLGN4X):c.1251G>C (p.Arg417=)	rs61741754	0.06453
NM_181332.3(NLGN4X):c.1777C>T (p.Leu593Phe)	rs3747333	0.00756
NM_181332.3(NLGN4X):c.2271G>A (p.Pro757=)	rs4999056	0.00609
NM_181332.3(NLGN4X):c.558C>T (p.Asp186=)	rs145911431	0.00414
NM_181332.3(NLGN4X):c.2280C>T (p.Tyr760=)	rs75350246	0.00384
NM_181332.3(NLGN4X):c.591C>T (p.Ile197=)	rs149003627	0.00101
NM_181332.3(NLGN4X):c.2223C>T (p.His741=)	rs541646409	0.00001
NM_181332.3(NLGN4X):c.1779C>G (p.Leu593=)	rs3747334

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