List of variants in gene FANCC reported as benign for Fanconi anemia complementation group C

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.521+109A>G	rs3737142	0.37815
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.77C>T (p.Ser26Phe)	rs1800361	0.00511
NM_000136.3(FANCC):c.-79+5G>A	rs4647350	0.00411
NM_000136.3(FANCC):c.-29A>C	rs4647414	0.00155
NM_000136.3(FANCC):c.457-18A>G	rs377206543	0.00036
NM_000136.3(FANCC):c.251-20T>C	rs370867462	0.00009

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