List of variants in gene FANCC reported as uncertain significance 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: 9

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.346-1930T>C	rs7850958	0.45701
NM_000136.3(FANCC):c.250+220G>A	rs356667	0.18637
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.346-47T>C	rs115475539	0.00153
NM_000136.3(FANCC):c.178G>A (p.Val60Ile)	rs138629441	0.00091
NM_000136.3(FANCC):c.388delinsAAAA (p.Glu130delinsLysLys)	rs1825721625
NM_000136.3(FANCC):c.8_9del (p.Gln3fs)	rs1831183107

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