List of variants in gene ATR reported as likely pathogenic by Invitae

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001184.4(ATR):c.2533-1G>A	rs755272769	0.00001
NM_001184.4(ATR):c.2634-1G>A	rs372271245	0.00001
NC_000003.11:g.(?_142168271)_(142226971_?)del
NC_000003.11:g.(?_142168271)_(142266772_?)del
NC_000003.11:g.(?_142231092)_(142232490_?)dup
NM_001184.4(ATR):c.1733-1G>A	rs2108478067
NM_001184.4(ATR):c.1885+1G>T
NM_001184.4(ATR):c.2342-1G>T
NM_001184.4(ATR):c.2976+1G>A	rs2108456024
NM_001184.4(ATR):c.3451-1G>A
NM_001184.4(ATR):c.4504-1G>C	rs910635641
NM_001184.4(ATR):c.4853-2A>G
NM_001184.4(ATR):c.6078+1G>C
NM_001184.4(ATR):c.6320-2A>C
NM_001184.4(ATR):c.7042-1G>A

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