List of variants in gene combination FANCA, LOC132090450 reported as benign for hematologic disorder

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.3408+45G>A	rs1800355	0.05862
NM_000135.4(FANCA):c.3408+33T>C	rs17227191	0.01875

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