List of variants in gene combination FANCA, LOC132090445, ZNF276 reported as pathogenic for Fanconi anemia complementation group A

Minimum submission review status:		Collection method:
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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.3828+1G>C	rs1432988639	0.00003
NM_000135.4(FANCA):c.3828+1G>T	rs1432988639
NM_000135.4(FANCA):c.3828+2dup	rs2062114186

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