List of variants in gene CR2 reported as benign by Invitae

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: 29

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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.2328T>C (p.Ile776=)	rs61735651	0.09124
NM_001006658.3(CR2):c.58+97G>A	rs1876453	0.08516
NM_001006658.3(CR2):c.3154A>G (p.Ile1052Val)	rs17618	0.07668
NM_001006658.3(CR2):c.1617C>T (p.Thr539=)	rs34349246	0.02179
NM_001006658.3(CR2):c.2649T>C (p.Gly883=)	rs1143665	0.02114
NM_001006658.3(CR2):c.635-20A>T	rs17045039	0.00789
NM_001006658.3(CR2):c.445+17A>G	rs145095346	0.00786
NM_001006658.3(CR2):c.1622G>T (p.Ser541Ile)	rs144075435	0.00520
NM_001006658.3(CR2):c.2240+19A>G	rs140933861	0.00357
NM_001006658.3(CR2):c.2352T>C (p.Ile784=)	rs142319454	0.00170
NM_001006658.3(CR2):c.2844G>A (p.Glu948=)	rs61754518	0.00098
NM_001006658.3(CR2):c.1978+7A>T	rs201274951	0.00068
NM_001006658.3(CR2):c.1494-17C>T	rs150388945	0.00031
NM_001006658.3(CR2):c.1395A>G (p.Gln465=)	rs188078143	0.00029
NM_001006658.3(CR2):c.200C>G (p.Thr67Ser)	rs45573035	0.00024
NM_001006658.3(CR2):c.2445A>G (p.Gly815=)	rs141282665	0.00024
NM_001006658.3(CR2):c.375C>T (p.Asn125=)	rs138096192	0.00018
NM_001006658.3(CR2):c.58+13G>A	rs373721952	0.00016
NM_001006658.3(CR2):c.2241-6C>T	rs200614122	0.00008
NM_001006658.3(CR2):c.1296A>T (p.Gly432=)	rs201585844
NM_001006658.3(CR2):c.3089-3del	rs1274247380
NM_001006658.3(CR2):c.3189-8_3189-7del	rs112859639
NM_001006658.3(CR2):c.624C>A (p.Pro208=)	rs61759494
NM_001006658.3(CR2):c.624C>G (p.Pro208=)	rs61759494

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