List of variants in gene ATM reported as not provided for not provided

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000051.4(ATM):c.1810C>T (p.Pro604Ser)	rs2227922	0.00431
NM_000051.4(ATM):c.3925G>A (p.Ala1309Thr)	rs149711770	0.00081
NM_000051.4(ATM):c.3014A>G (p.Asn1005Ser)	rs146531614	0.00028
NM_000051.4(ATM):c.4414T>G (p.Leu1472Val)	rs539676759	0.00009
NM_000051.4(ATM):c.749G>A (p.Arg250Gln)	rs56123940	0.00007
NM_000051.4(ATM):c.1339C>T (p.Arg447Ter)	rs587779815	0.00001
NM_000051.4(ATM):c.1880T>G (p.Phe627Cys)	rs546087885	0.00001
NM_000051.4(ATM):c.496+3A>G	rs876658311	0.00001
NM_000051.4(ATM):c.2922-2A>T	rs1591603471
NM_000051.4(ATM):c.3245_3247delinsTGAT (p.His1082fs)	rs587776549

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