List of variants in gene ATR reported as benign by Eurofins NTD LLC (GA)

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001184.4(ATR):c.7875G>A (p.Gln2625=)	rs1802904	0.88595
NM_001184.4(ATR):c.1776T>A (p.Gly592=)	rs2227930	0.63717
NM_001184.4(ATR):c.632T>C (p.Met211Thr)	rs2227928	0.63625
NM_001184.4(ATR):c.1815T>C (p.Asp605=)	rs2227929	0.33689
NM_001184.4(ATR):c.5739-7_5739-6del	rs72371423	0.01173
NM_001184.4(ATR):c.4153-21dup	rs112116713
NM_001184.4(ATR):c.5739-14_5739-9del	rs72272981

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