List of variants in gene combination FANCA, LOC112486223 reported as benign for Fanconi anemia complementation group A

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.17T>A (p.Val6Asp)	rs1800282	0.06490
NM_000135.4(FANCA):c.24C>G (p.Asn8Lys)	rs76275444	0.04436
NM_000135.4(FANCA):c.21G>T (p.Pro7=)	rs115856189	0.00509

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