ClinVar Miner

List of variants in gene combination CR2, LOC126805994 reported as uncertain significance by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001006658.3(CR2):c.970C>T (p.Arg324Cys)	rs147393483	0.00050
NM_001006658.3(CR2):c.1210C>G (p.Pro404Ala)	rs148388565	0.00034

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