List of variants in gene combination FANCG, VCP reported as benign for immune system disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_004629.2(FANCG):c.1636+7A>G	rs587118	0.35683
NM_004629.2(FANCG):c.1133C>T (p.Ser378Leu)	rs4986939	0.03269
NM_004629.2(FANCG):c.890C>T (p.Thr297Ile)	rs2237857	0.02968
NM_004629.2(FANCG):c.1538G>A (p.Arg513Gln)	rs17885240	0.00863
NM_004629.2(FANCG):c.640C>T (p.Arg214Cys)	rs61757385	0.00285
NM_004629.2(FANCG):c.1638T>C (p.Gly546=)	rs45537335	0.00175

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