List of variants in gene NOTCH1 reported as benign by Fulgent Genetics, Fulgent Genetics

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_017617.5(NOTCH1):c.711C>T (p.Gly237=)	rs61751557	0.01860
NM_017617.5(NOTCH1):c.2205C>T (p.Asn735=)	rs2229970	0.01759
NM_017617.5(NOTCH1):c.4129C>T (p.Pro1377Ser)	rs61751542	0.01473
NM_017617.5(NOTCH1):c.5679C>T (p.Gly1893=)	rs2229973	0.01198
NM_017617.5(NOTCH1):c.5011G>A (p.Val1671Ile)	rs2229968	0.00847
NM_017617.5(NOTCH1):c.1635C>T (p.Asp545=)	rs11574889	0.00824
NM_017617.5(NOTCH1):c.5124G>T (p.Ser1708=)	rs35980907	0.00561
NM_017617.5(NOTCH1):c.2049G>A (p.Ala683=)	rs61751553	0.00096

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