List of variants in gene FANCG reported as pathogenic by OMIM

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_004629.2(FANCG):c.1480+1G>C	rs149616199	0.00002
NM_004629.2(FANCG):c.313G>T (p.Glu105Ter)	rs121434425	0.00001
NM_004629.1(FANCG):c.1795_1804del (p.Trp599Profs)	rs397507560
NM_004629.2(FANCG):c.1066C>T (p.Gln356Ter)	rs121434426
NM_004629.2(FANCG):c.1761-1G>C	rs1829035889
NM_004629.2(FANCG):c.307+1G>C	rs200479612
NM_004629.2(FANCG):c.637_643del (p.Tyr213fs)	rs587776640
NM_004629.2(FANCG):c.925-2A>G	rs397507561

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