ClinVar Miner

List of variants reported as pathogenic for CHEK2-related cancer predisposition by Rady Children's Institute for Genomic Medicine, Rady Children's Hospital San Diego

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.1100del (p.Thr367fs)	rs555607708	0.00181
NM_007194.4(CHEK2):c.444+1G>A	rs121908698	0.00009

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