List of variants studied for Fanconi anemia complementation group J by St. Jude Molecular Pathology, St. Jude Children's Research Hospital

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_032043.3(BRIP1):c.2392C>T (p.Arg798Ter)	rs137852986	0.00010
NM_032043.3(BRIP1):c.2863A>C (p.Asn955His)	rs587782244	0.00005
NM_032043.3(BRIP1):c.1641T>G (p.Asp547Glu)	rs754414731	0.00001
NM_032043.3(BRIP1):c.2935A>G (p.Lys979Glu)	rs730881627	0.00001
NM_032043.3(BRIP1):c.2170A>C (p.Ile724Leu)	rs2077032430

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