List of variants in gene FANCM reported as likely pathogenic for FANCM-related disorder

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_020937.4(FANCM):c.5101C>T (p.Gln1701Ter)	rs147021911	0.00104
NM_020937.4(FANCM):c.1972C>T (p.Arg658Ter)	rs368728266	0.00009
NM_020937.4(FANCM):c.1879C>T (p.Arg627Ter)	rs374626826	0.00001
NM_020937.4(FANCM):c.5221dup (p.Thr1741fs)	rs758498345	0.00001
NM_020937.4(FANCM):c.107del (p.Gly36fs)
NM_020937.4(FANCM):c.1405_1406del (p.Thr469fs)
NM_020937.4(FANCM):c.466C>T (p.Gln156Ter)	rs1885521004
NM_020937.4(FANCM):c.5047A>T (p.Lys1683Ter)	rs1213350464
NM_020937.4(FANCM):c.5315_5316del (p.Asp1771_Cys1772insTer)	rs1566783809

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