List of variants in gene LRIG1 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_015541.3(LRIG1):c.70C>G (p.Leu24Val)	rs1403626	0.77161
NM_015541.3(LRIG1):c.76C>G (p.Leu26Val)	rs1403625	0.75533
NM_015541.3(LRIG1):c.2221T>C (p.Leu741=)	rs900171	0.62545
NM_015541.3(LRIG1):c.1317C>T (p.Ser439=)	rs6793110	0.30941
NM_015541.3(LRIG1):c.1843A>G (p.Met615Val)	rs2306272	0.24919
NM_015541.3(LRIG1):c.3158A>C (p.Gln1053Pro)	rs2279290	0.16583

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