List of variants in gene combination FANCA, ZNF276 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001113525.2(ZNF276):c.1574+17del	rs375657470	0.04486
NM_000135.4(FANCA):c.3859G>A (p.Val1287Ile)	rs17227354	0.02526
NM_000135.4(FANCA):c.3891G>A (p.Lys1297=)	rs17227361	0.00286
NM_001113525.2(ZNF276):c.1575-29G>A	rs17227438	0.00151
NM_000135.4(FANCA):c.4036G>A (p.Ala1346Thr)	rs17227396	0.00056
NM_001113525.2(ZNF276):c.*1313A>G	rs368376237	0.00012
NM_001113525.2(ZNF276):c.1574+26del	rs66471129

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