List of variants in gene combination FANCF, LOC130005443 reported as uncertain significance for bone marrow disorder

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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: 24

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HGVS	dbSNP	gnomAD frequency
NM_022725.4(FANCF):c.1087C>T (p.Gln363Ter)	rs201285915	0.00010
NM_022725.4(FANCF):c.970A>G (p.Lys324Glu)	rs200416138	0.00008
NM_022725.4(FANCF):c.1048C>T (p.Leu350Phe)	rs368170054	0.00004
NM_022725.4(FANCF):c.1012G>A (p.Asp338Asn)	rs149687560	0.00003
NM_022725.4(FANCF):c.986T>C (p.Leu329Pro)	rs766964364	0.00002
NM_022725.4(FANCF):c.1056A>C (p.Leu352Phe)	rs754545069	0.00001
NM_022725.4(FANCF):c.1060C>T (p.Leu354Phe)	rs1858614394	0.00001
NM_022725.4(FANCF):c.1078A>G (p.Arg360Gly)	rs1357749824	0.00001
NM_022725.4(FANCF):c.1001C>T (p.Ala334Val)	rs772941983
NM_022725.4(FANCF):c.1006G>A (p.Asp336Asn)	rs886048157
NM_022725.4(FANCF):c.1007A>G (p.Asp336Gly)	rs2133796304
NM_022725.4(FANCF):c.1025C>T (p.Pro342Leu)
NM_022725.4(FANCF):c.1041G>A (p.Trp347Ter)	rs587778343
NM_022725.4(FANCF):c.1048C>A (p.Leu350Ile)
NM_022725.4(FANCF):c.1063C>T (p.Arg355Cys)	rs1858614312
NM_022725.4(FANCF):c.1064G>A (p.Arg355His)	rs758175326
NM_022725.4(FANCF):c.1082A>G (p.Lys361Arg)	rs2133796173
NM_022725.4(FANCF):c.1089A>C (p.Gln363His)	rs1858613638
NM_022725.4(FANCF):c.940C>T (p.Leu314Phe)	rs1858617232
NM_022725.4(FANCF):c.943dup (p.Cys315fs)	rs1590540654
NM_022725.4(FANCF):c.952C>G (p.Pro318Ala)
NM_022725.4(FANCF):c.952C>T (p.Pro318Ser)	rs746120363
NM_022725.4(FANCF):c.992C>T (p.Thr331Ile)	rs1250903119
NM_022725.4(FANCF):c.994T>C (p.Cys332Arg)

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