List of variants in gene ATM reported as likely pathogenic by Cancer Genomics Group, Japanese Foundation For Cancer Research

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.1122_1123del (p.Glu376fs)	rs1591517571
NM_000051.4(ATM):c.242dup (p.Asn81fs)	rs1591451795
NM_000051.4(ATM):c.4776+2T>A	rs587781927
NM_000051.4(ATM):c.5511_5512del (p.Phe1837fs)	rs1555107263

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