ClinVar Miner

List of variants in gene FANCM reported as pathogenic by Laan Lab, Human Genetics Research Group, University of Tartu

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: 2

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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.1491dup (p.Gln498fs)	rs797045116	0.00005

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