List of variants in gene FANCM reported as benign by Genetic Services Laboratory, University of Chicago

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_020937.4(FANCM):c.5190G>A (p.Gln1730=)	rs7142192	0.00869
NM_020937.4(FANCM):c.3863A>G (p.Asn1288Ser)	rs116519044	0.00868
NM_020937.4(FANCM):c.5656C>T (p.His1886Tyr)	rs79343837	0.00824
NM_020937.4(FANCM):c.2445G>A (p.Ser815=)	rs61745871	0.00750
NM_020937.4(FANCM):c.4563A>C (p.Glu1521Asp)	rs113986680	0.00382
NM_020937.4(FANCM):c.3040G>T (p.Gly1014Cys)	rs77532752	0.00375
NM_020937.4(FANCM):c.527C>T (p.Thr176Ile)	rs77374493	0.00371
NM_020937.4(FANCM):c.5577T>C (p.Asn1859=)	rs113831595	0.00292
NM_020937.4(FANCM):c.2749A>G (p.Ile917Val)	rs148871932	0.00287
NM_020937.4(FANCM):c.171G>C (p.Leu57Phe)	rs142007602	0.00161
NM_020937.4(FANCM):c.1041G>A (p.Pro347=)	rs140998495	0.00147

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