ClinVar Miner

List of variants studied for Fanconi anemia complementation group A by Genetics and Genomic Medicine Centre, NeuroGen Healthcare, NeuroGen Healthcare

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.2T>C (p.Met1Thr)	rs769479800	0.00004
NM_000135.4(FANCA):c.1979T>C (p.Leu660Pro)	rs1567621042

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