List of variants in gene combination AOPEP, FANCC reported as likely benign for Fanconi anemia complementation group A

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000136.3(FANCC):c.1394A>G (p.Gln465Arg)	rs1800368	0.00361
NM_000136.3(FANCC):c.584A>T (p.Asp195Val)	rs1800365	0.00275
NM_000136.3(FANCC):c.1156T>C (p.Ser386Pro)	rs41281202	0.00236
NM_000136.3(FANCC):c.632C>G (p.Pro211Arg)	rs140781259	0.00126
NM_000136.3(FANCC):c.554G>A (p.Arg185Gln)	rs370346767	0.00009
NM_000136.3(FANCC):c.1161C>T (p.Cys387=)	rs548998258	0.00002
NM_000136.3(FANCC):c.1155-29A>G	rs759352163	0.00001
NM_000136.3(FANCC):c.1275C>G (p.Leu425=)	rs767126985	0.00001
NM_000136.3(FANCC):c.1534-18C>T	rs1289718209	0.00001
NM_000136.3(FANCC):c.1329+10A>G	rs977427150
NM_000136.3(FANCC):c.687-5G>T	rs767811745
NM_000136.3(FANCC):c.844-10_844-8del	rs758617953

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