List of variants in gene FANCA reported as likely benign by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.542C>T (p.Ala181Val)	rs17232246	0.04972
NM_000135.4(FANCA):c.755A>G (p.Asp252Gly)	rs17225943	0.01851
NM_000135.4(FANCA):c.601C>T (p.Pro201Ser)	rs144917960	0.00895
NM_000135.4(FANCA):c.2574C>G (p.Ser858Arg)	rs17233141	0.00567
NM_000135.4(FANCA):c.932T>C (p.Ile311Thr)	rs75501942	0.00334
NM_000135.4(FANCA):c.857A>G (p.Gln286Arg)	rs13336566	0.00303
NM_000135.4(FANCA):c.1830A>G (p.Ala610=)	rs1800338	0.00201
NM_000135.4(FANCA):c.3412C>G (p.Leu1138Val)	rs138417003	0.00041
NM_000135.4(FANCA):c.2236G>T (p.Ala746Ser)	rs575108446	0.00011
NM_000135.4(FANCA):c.3114C>T (p.Leu1038=)	rs55758861	0.00009
NM_000135.4(FANCA):c.3538G>A (p.Val1180Met)	rs372706571	0.00001
NM_000135.4(FANCA):c.1901-3C>A	rs17226526
NM_000135.4(FANCA):c.3265G>A (p.Val1089Ile)	rs536839082

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