List of variants in gene NIPBL reported as benign by Athena Diagnostics Inc

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_133433.4(NIPBL):c.2021A>G (p.Asn674Ser)	rs3822471	0.12117
NM_133433.4(NIPBL):c.4421+7A>G	rs76297333	0.02109
NM_133433.4(NIPBL):c.4561-9T>A	rs79924167	0.02103
NM_133433.4(NIPBL):c.1965G>T (p.Glu655Asp)	rs80358350	0.00379
NM_133433.4(NIPBL):c.6109-3T>C	rs145778995	0.00354
NM_133433.4(NIPBL):c.3897T>C (p.Leu1299=)	rs80358354	0.00280
NM_133433.4(NIPBL):c.4245A>C (p.Ser1415=)	rs138440449	0.00229
NM_133433.4(NIPBL):c.7830G>C (p.Val2610=)	rs115668015	0.00186
NM_133433.4(NIPBL):c.8337G>A (p.Thr2779=)	rs139108785	0.00047
NM_133433.4(NIPBL):c.198C>G (p.Val66=)	rs146033170	0.00036
NM_133433.4(NIPBL):c.3861C>T (p.Asn1287=)	rs531615496	0.00006

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