List of variants in gene NRXN1 reported as benign by PreventionGenetics, part of Exact Sciences

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001330078.2(NRXN1):c.3364+20T>C	rs3213756	0.25608
NM_001330078.2(NRXN1):c.511C>T (p.Leu171=)	rs1045874	0.17452
NM_001330078.2(NRXN1):c.900C>T (p.Pro300=)	rs2303298	0.01844
NM_001330078.2(NRXN1):c.4068G>A (p.Thr1356=)	rs74714098	0.01437
NM_001330078.2(NRXN1):c.2421C>T (p.Asn807=)	rs115211871	0.00535
NM_001330078.2(NRXN1):c.1285C>T (p.Pro429Ser)	rs78540316	0.00323
NM_001330078.2(NRXN1):c.2605C>A (p.Leu869Met)	rs201818223	0.00044
NM_001330078.2(NRXN1):c.832+1873C>T
NM_001330078.2(NRXN1):c.832+2687C>T
NM_138735.4(NRXN1):c.49[5] (p.Gly17[5])	rs750165040

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