List of variants in gene CR2 reported 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
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_001006658.3(CR2):c.3185C>A (p.Ala1062Glu)	rs17617	0.88540
NM_001006658.3(CR2):c.1776G>A (p.Leu592=)	rs1048971	0.42495
NM_001006658.3(CR2):c.1987T>C (p.Ser663Pro)	rs4308977	0.32718
NM_001006658.3(CR2):c.1916G>A (p.Ser639Asn)	rs17615	0.30786
NM_001006658.3(CR2):c.2012G>A (p.Arg671His)	rs17616	0.30700
NM_001006658.3(CR2):c.524C>T (p.Pro175Leu)	rs75282758

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