List of variants in gene combination FANCA, ZNF276 reported as 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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001113525.2(ZNF276):c.1574+23del	rs17233826	0.48664
NM_000135.4(FANCA):c.3807G>C (p.Leu1269=)	rs11649210	0.11105
NM_000135.4(FANCA):c.3982A>G (p.Thr1328Ala)	rs9282681	0.05868
NM_001113525.2(ZNF276):c.1475-191C>T	rs16966023	0.04351
NM_001113525.2(ZNF276):c.1574+23T>C	rs62704561	0.03426
NM_001113525.2(ZNF276):c.*103C>G	rs17233797	0.03296
NM_001113525.2(ZNF276):c.1815G>C (p.Glu605Asp)	rs17227424	0.02929
NM_001113525.2(ZNF276):c.*68C>T	rs17227417	0.02259
NM_001113525.2(ZNF276):c.1574+26C>A	rs17233812	0.01850
NM_001113525.2(ZNF276):c.1475-216G>A	rs17227452	0.01670
NM_001113525.2(ZNF276):c.1574+17A>C	rs17233833	0.01627
NM_001113525.2(ZNF276):c.*1316C>T	rs9282680	0.01028
NM_000135.4(FANCA):c.4332T>G (p.Pro1444=)	rs149531696	0.00072
NM_001113525.2(ZNF276):c.*69G>A	rs17233804	0.00019
NM_001113525.2(ZNF276):c.*201C>T	rs1230

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