ClinVar Miner

List of variants reported as uncertain significance for encephalopathy, acute, infection-induced by Baylor Genetics

Included ClinVar conditions (1):

Familial acute necrotizing encephalopathy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_006267.5(RANBP2):c.3363G>T (p.Lys1121Asn)	rs112835359
NM_006267.5(RANBP2):c.7125C>A (p.Asp2375Glu)	rs1332179032
NM_006267.5(RANBP2):c.775C>G (p.Leu259Val)	rs1695576898

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