List of variants in gene combination FANCL, VRK2 reported as likely benign for anemia

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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: 15

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HGVS	dbSNP	gnomAD frequency
NM_018062.4(FANCL):c.1115G>C (p.Gly372Ala)	rs149803148	0.00121
NM_018062.4(FANCL):c.*333A>G	rs147811379	0.00076
NM_018062.4(FANCL):c.1124A>C (p.His375Pro)	rs545084971	0.00008
NM_018062.4(FANCL):c.1093-19_1093-9dup	rs771654902	0.00001
NM_018062.4(FANCL):c.1093-34_1093-16del	rs760337641	0.00001
NM_006296.7(VRK2):c.102_105dup	rs759217526
NM_018062.4(FANCL):c.1093-10C>A
NM_018062.4(FANCL):c.1093-10_1093-8del
NM_018062.4(FANCL):c.1093-11T>A
NM_018062.4(FANCL):c.1093-12C>G
NM_018062.4(FANCL):c.1093-13T>C
NM_018062.4(FANCL):c.1093-15G>A
NM_018062.4(FANCL):c.1093-15G>T	rs767450055
NM_018062.4(FANCL):c.1093-17A>T
NM_018062.4(FANCL):c.1093-18T>G

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