List of variants in gene FANCC reported as likely pathogenic by Baylor Genetics

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.125dup (p.Glu43fs)
NM_000136.3(FANCC):c.163del (p.Met55fs)
NM_000136.3(FANCC):c.169del (p.Ser57fs)
NM_000136.3(FANCC):c.220del (p.Ala74fs)	rs1588350264
NM_000136.3(FANCC):c.267del (p.Ile89_Leu90insTer)	rs777918411
NM_000136.3(FANCC):c.275G>A (p.Trp92Ter)	rs1830584796
NM_000136.3(FANCC):c.276G>A (p.Trp92Ter)
NM_000136.3(FANCC):c.29dup (p.Cys10fs)	rs878853671
NM_000136.3(FANCC):c.345+1del	rs1057516247
NM_000136.3(FANCC):c.346-1G>A	rs1484503633
NM_000136.3(FANCC):c.346-1G>C
NM_000136.3(FANCC):c.362_363del (p.Ile121fs)	rs1588220728
NM_000136.3(FANCC):c.387_390del (p.Glu130fs)
NM_000136.3(FANCC):c.457-2A>G
NM_000136.3(FANCC):c.507del (p.Phe169fs)	rs1588218493
NM_000136.3(FANCC):c.5dup (p.Gln3fs)	rs1268491295

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