List of variants in gene LRIG2 reported as uncertain significance by Gharavi Laboratory, Columbia University

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_014813.3(LRIG2):c.1657C>T (p.Gln553Ter)	rs1557914388
NM_014813.3(LRIG2):c.2087C>A (p.Pro696His)	rs1557917271
NM_014813.3(LRIG2):c.2476del (p.Ile826fs)	rs1557918089
NM_014813.3(LRIG2):c.3132del (p.Arg1044fs)	rs1557924687
NM_014813.3(LRIG2):c.3G>A (p.Met1Ile)	rs1557891106
NM_014813.3(LRIG2):c.993del (p.Phe331fs)	rs1326615116

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