ClinVar Miner

List of variants in gene INF2 reported by Equipe Genetique des Anomalies du Developpement, Université de Bourgogne

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_022489.4(INF2):c.167G>A (p.Arg56His)	rs1595163730
NM_022489.4(INF2):c.310T>C (p.Cys104Arg)	rs387907034

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