List of variants in gene AMER1 reported as pathogenic by Genomic Center, National Cancer Institute

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_152424.4(AMER1):c.2422_2423insG (p.Thr808fs)	rs1930230724
NM_152424.4(AMER1):c.3226A>T (p.Lys1076Ter)	rs1930207901
NM_152424.4(AMER1):c.640del (p.Val214fs)	rs1930277434

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