List of variants in gene FANCF reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_022725.4(FANCF):c.373G>A (p.Asp125Asn)	rs61752920	0.00605
NM_022725.4(FANCF):c.199A>C (p.Arg67=)	rs146647469	0.00325
NM_022725.4(FANCF):c.241G>T (p.Ala81Ser)	rs145057187	0.00048
NM_022725.4(FANCF):c.687A>T (p.Ser229=)	rs776140806	0.00021
NM_022725.4(FANCF):c.465A>T (p.Pro155=)	rs201215734	0.00020
NM_022725.4(FANCF):c.148C>T (p.Arg50Trp)	rs577253174	0.00006
NM_022725.4(FANCF):c.873A>G (p.Lys291=)	rs757578045	0.00005
NM_022725.4(FANCF):c.360C>T (p.Gly120=)	rs775422716	0.00004
NM_022725.4(FANCF):c.234G>A (p.Pro78=)	rs144503236	0.00003
NM_022725.4(FANCF):c.24G>C (p.Leu8=)	rs1035401874	0.00001
NM_022725.4(FANCF):c.675C>T (p.Gly225=)	rs767689033	0.00001

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