Variants in gene combination FANCA, ZNF276 with conflicting interpretations reported as "likely benign and "benign"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status:		Submission 2 (benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 8

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.3859G>A (p.Val1287Ile)	rs17227354	0.02526
NM_001113525.2(ZNF276):c.*1316C>T	rs9282680	0.01028
NM_000135.4(FANCA):c.4249C>G (p.His1417Asp)	rs17227403	0.00362
NM_000135.4(FANCA):c.3891G>A (p.Lys1297=)	rs17227361	0.00286
NM_000135.4(FANCA):c.4332T>G (p.Pro1444=)	rs149531696	0.00072
NM_000135.4(FANCA):c.4036G>A (p.Ala1346Thr)	rs17227396	0.00056
NM_001113525.2(ZNF276):c.*1313A>G	rs368376237	0.00012
NM_000135.4(FANCA):c.4226G>A (p.Arg1409Gln)	rs370507983	0.00006

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