Variants in gene FANCC with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status:		Submission 1 (likely benign) 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.408A>G (p.Gln136=)	rs1800360	0.02397
NM_000136.3(FANCC):c.416G>A (p.Gly139Glu)	rs1800362	0.01494
NM_000136.3(FANCC):c.-155A>C	rs549658720	0.00998
NM_000136.3(FANCC):c.77C>T (p.Ser26Phe)	rs1800361	0.00511
NM_000136.3(FANCC):c.178G>A (p.Val60Ile)	rs138629441	0.00091
NM_000136.3(FANCC):c.29G>A (p.Cys10Tyr)	rs143152201	0.00019
NM_000136.3(FANCC):c.345+6A>T	rs368595927	0.00007
NM_000136.3(FANCC):c.395C>G (p.Ala132Gly)	rs587779905	0.00005
NM_000136.3(FANCC):c.438T>C (p.Tyr146=)	rs765990832	0.00003
NM_000136.3(FANCC):c.345+4AG[2]	rs755657969

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