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

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Total variants: 10

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.1826+12C>T	rs183513839	0.00514
NM_000135.4(FANCA):c.4249C>G (p.His1417Asp)	rs17227403	0.00349
NM_000135.4(FANCA):c.1471-12A>G	rs9282684	0.00163
NM_000135.4(FANCA):c.2658G>C (p.Glu886Asp)	rs139002130	0.00055
NM_000135.4(FANCA):c.3430C>T (p.Arg1144Trp)	rs143671872	0.00046
NM_000135.4(FANCA):c.3412C>G (p.Leu1138Val)	rs138417003	0.00041
NM_000135.4(FANCA):c.2390C>T (p.Ala797Val)	rs138248569	0.00026
NM_000135.4(FANCA):c.1756G>A (p.Ala586Thr)	rs201212806	0.00006
NM_000135.4(FANCA):c.624G>A (p.Ser208=)	rs922099383	0.00002
NM_000135.4(FANCA):c.1380A>G (p.Arg460=)	rs1035276734	0.00001

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