List of variants in gene combination FANCM, LOC130055524 reported as uncertain significance for hematologic 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_020937.4(FANCM):c.53G>A (p.Arg18Gln)	rs146609069	0.00011
NM_020937.4(FANCM):c.56C>T (p.Ser19Leu)	rs201383385	0.00003
NM_020937.4(FANCM):c.68C>A (p.Pro23Gln)	rs377031191	0.00003
NM_020937.4(FANCM):c.88G>C (p.Glu30Gln)	rs373268822	0.00002
NM_020937.4(FANCM):c.98A>G (p.Gln33Arg)	rs759911498	0.00001
NC_000014.8:g.(?_45605225)_(45609922_?)dup
NM_020937.4(FANCM):c.70G>C (p.Gly24Arg)
NM_020937.4(FANCM):c.71G>T (p.Gly24Val)	rs1885468827
NM_020937.4(FANCM):c.80C>T (p.Ser27Phe)	rs1885469771
NM_020937.4(FANCM):c.83G>T (p.Gly28Val)	rs1885470299
NM_020937.4(FANCM):c.95C>T (p.Pro32Leu)
NM_020937.4(FANCM):c.98A>C (p.Gln33Pro)

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