List of variants in gene JAG1 reported as likely 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000214.3(JAG1):c.2810G>A (p.Arg937Gln)	rs145895196	0.00180
NM_000214.3(JAG1):c.2301G>A (p.Thr767=)	rs147634857	0.00165
NM_000214.3(JAG1):c.909T>C (p.His303=)	rs139574260	0.00121
NM_000214.3(JAG1):c.1120+10A>G	rs201711717	0.00118
NM_000214.3(JAG1):c.1578C>T (p.Ile526=)	rs1801139	0.00092
NM_000214.3(JAG1):c.439+10G>A	rs201371037	0.00081
NM_000214.3(JAG1):c.2231G>A (p.Arg744Gln)	rs147809756	0.00069
NM_000214.3(JAG1):c.1389C>T (p.Ser463=)	rs147229008	0.00050
NM_000214.3(JAG1):c.894T>C (p.Asn298=)	rs149897344	0.00039
NM_000214.3(JAG1):c.3296C>T (p.Pro1099Leu)	rs200949270	0.00023
NM_000214.3(JAG1):c.1806C>T (p.His602=)	rs764290237	0.00015
NM_000214.3(JAG1):c.1043G>A (p.Arg348Lys)	rs200227737	0.00014
NM_000214.3(JAG1):c.526G>A (p.Val176Ile)	rs199674138	0.00013
NM_000214.3(JAG1):c.1655C>T (p.Pro552Leu)	rs201785359	0.00006

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