ClinVar Miner

List of variants in gene CR2 reported by Neuberg Centre For Genomic Medicine, NCGM

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001006658.3(CR2):c.202A>G (p.Lys68Glu)	rs771267937	0.00002
NM_001006658.3(CR2):c.1282C>T (p.Arg428Cys)	rs373176986	0.00001
NM_001006658.3(CR2):c.2495G>A (p.Ser832Asn)	rs775501900

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