List of variants in gene NRXN1 studied for History of neurodevelopmental disorder

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_001330078.2(NRXN1):c.4068G>A (p.Thr1356=)	rs74714098	0.01437
NM_001330078.2(NRXN1):c.3408G>A (p.Thr1136=)	rs80094872	0.00737
NM_001330078.2(NRXN1):c.3933A>G (p.Ala1311=)	rs79970751	0.00503
NM_001330078.2(NRXN1):c.4473G>A (p.Ala1491=)	rs113380721	0.00191
NM_001330078.2(NRXN1):c.4254A>G (p.Pro1418=)	rs55923848	0.00109
NM_001330078.2(NRXN1):c.4275G>T (p.Arg1425=)	rs143495349	0.00096
NM_001330078.2(NRXN1):c.4392T>C (p.His1464=)	rs112536447	0.00035
NM_001330078.2(NRXN1):c.4248G>A (p.Pro1416=)	rs151195816	0.00006
NM_001330078.2(NRXN1):c.3919G>A (p.Val1307Ile)	rs200044811	0.00001
NM_001330078.2(NRXN1):c.4405C>A (p.Arg1469=)	rs1331703447

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