Variants in gene combination FANCA, ZNF276 with conflicting interpretations reported as "pathogenic and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000135.4(FANCA):c.4249C>G (p.His1417Asp)	rs17227403	0.00362
NM_000135.4(FANCA):c.4199G>A (p.Arg1400His)	rs149851163	0.00003
NM_000135.4(FANCA):c.4085T>A (p.Leu1362Ter)	rs745688750	0.00001
NM_000135.4(FANCA):c.3878del (p.Glu1293fs)	rs2062089336
NM_000135.4(FANCA):c.3884T>G (p.Leu1295Ter)	rs986710868
NM_000135.4(FANCA):c.3904T>C (p.Trp1302Arg)	rs878853665
NM_000135.4(FANCA):c.4075G>T (p.Asp1359Tyr)	rs1555533313
NM_000135.4(FANCA):c.4261-2A>G	rs915983602
NM_001113525.2(ZNF276):c.474_481del	rs1567591276

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