List of variants in gene FANCC reported as pathogenic by Leiden Open Variation Database

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.456+4A>T	rs104886456	0.00021
NM_000136.3(FANCC):c.521+1G>A	rs145394391	0.00004
NM_000136.3(FANCC):c.520C>T (p.Arg174Ter)	rs781542763	0.00002
NM_000136.3(FANCC):c.65G>A (p.Trp22Ter)	rs377294947	0.00002
NM_000136.3(FANCC):c.37C>T (p.Gln13Ter)	rs121917784	0.00001
NC_000009.12:g.(95172148_95240648)_(95240744_95247431)del
NC_000009.12:g.(95240744_95247431)_(95317709_?)del
NM_000136.3(FANCC):c.165+1G>T	rs794726668
NM_000136.3(FANCC):c.166-620_250+3083delinsAACTAAATTTACTTTTT
NM_000136.3(FANCC):c.338G>A (p.Trp113Ter)	rs1064793405
NM_000136.3(FANCC):c.346-1G>A	rs1484503633
NM_000136.3(FANCC):c.355_360delinsA (p.Ser119fs)	rs587779904
NM_000136.3(FANCC):c.356_360del (p.Ser119fs)	rs1060499606
NM_000136.3(FANCC):c.377_378del (p.Arg126fs)	rs1564720637
NM_000136.3(FANCC):c.455dup (p.Asn152fs)	rs774170058
NM_000136.3(FANCC):c.467del (p.Ser156fs)	rs1825652623
NM_000136.3(FANCC):c.487_490del (p.Glu163fs)	rs730881708
NM_000136.3(FANCC):c.489_490del (p.Asn164fs)	rs730881708

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