List of variants reported as pathogenic for Fanconi anemia complementation group A by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.2T>C (p.Met1Thr)	rs769479800	0.00005
GRCh38/hg38 16q24.3(chr16:89764114-89781847)x0
NM_000135.4(FANCA):c.1492del (p.Leu498fs)	rs2544243740
NM_000135.4(FANCA):c.4010+1_4010+18del	rs752457319

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