List of variants in gene FANCM reported as benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_020937.4(FANCM):c.6141T>C (p.Asp2047=)	rs8018014	0.03012
NM_020937.4(FANCM):c.3758A>G (p.Asn1253Ser)	rs45604036	0.02189
NM_020937.4(FANCM):c.5627A>G (p.Asn1876Ser)	rs45557033	0.02173
NM_020937.4(FANCM):c.229A>G (p.Thr77Ala)	rs61746895	0.01981
NM_020937.4(FANCM):c.4799C>T (p.Thr1600Ile)	rs61746943	0.01614
NM_020937.4(FANCM):c.5224A>G (p.Ile1742Val)	rs143662421	0.00811

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