ClinVar Miner

List of variants studied for Fanconi anemia complementation group J by Neuberg Centre For Genomic Medicine, NCGM

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Total variants: 2

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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.62C>A (p.Ala21Asp)	rs1603368436

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