List of variants in gene DLG5 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004747.4(DLG5):c.2223C>T (p.Ala741=)	rs35323061	0.00398
NM_004747.4(DLG5):c.4819G>A (p.Asp1607Asn)	rs147733899	0.00387
NM_004747.4(DLG5):c.2345G>A (p.Arg782His)	rs146507058	0.00247
NM_004747.4(DLG5):c.3200G>A (p.Arg1067His)	rs201354863	0.00059
NM_004747.4(DLG5):c.1406C>T (p.Ala469Val)
NM_004747.4(DLG5):c.2526G>A (p.Thr842=)
NM_004747.4(DLG5):c.2795C>G (p.Ser932Cys)

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