List of variants in gene DNA2 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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_001080449.3(DNA2):c.2713C>A (p.Gln905Lys)	rs181679245	0.00459
NM_001080449.3(DNA2):c.2153G>T (p.Cys718Phe)	rs147096750	0.00367
NM_001080449.3(DNA2):c.2826G>A (p.Pro942=)	rs200956547	0.00011
NM_001080449.3(DNA2):c.264T>C (p.Ser88=)	rs749078276	0.00009
NM_001080449.3(DNA2):c.1677G>A (p.Leu559=)	rs769027938	0.00004
NM_001080449.3(DNA2):c.1415+8G>A	rs564046796	0.00001
NM_001080449.3(DNA2):c.27G>A (p.Leu9=)	rs1211027535	0.00001
NM_001080449.3(DNA2):c.1041C>T (p.Asn347=)
NM_001080449.3(DNA2):c.1722A>G (p.Pro574=)
NM_001080449.3(DNA2):c.1827T>A (p.Ser609=)
NM_001080449.3(DNA2):c.2322C>T (p.Gly774=)
NM_001080449.3(DNA2):c.2955T>C (p.Asn985=)
NM_001080449.3(DNA2):c.3087G>C (p.Leu1029=)
NM_001080449.3(DNA2):c.3099A>G (p.Leu1033=)
NM_001080449.3(DNA2):c.791G>A (p.Ser264Asn)

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