ClinVar Miner

List of variants reported as likely benign for Fanconi anemia complementation group J by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.3099T>C (p.Pro1033=)	rs202228407	0.00013
NM_032043.3(BRIP1):c.1626C>T (p.Ser542=)	rs373709958	0.00004

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