Variants in gene FANCM with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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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.5791C>T (p.Arg1931Ter)	rs144567652	0.00088
NM_020937.4(FANCM):c.4318-1G>A	rs752228025	0.00008
NM_020937.4(FANCM):c.1060C>T (p.Gln354Ter)	rs1156577591	0.00001

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