List of variants in gene FANCG reported as not provided 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_004629.2(FANCG):c.1367A>T (p.His456Leu)	rs148808709	0.00013
NM_004629.2(FANCG):c.1480+1G>C	rs149616199	0.00002
NM_004629.2(FANCG):c.1183_1192del (p.Glu395fs)	rs397507559
NM_004629.2(FANCG):c.307+1G>C	rs200479612
NM_004629.2(FANCG):c.925-2A>G	rs397507561

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