List of variants in gene combination ACTC1, GJD2-DT 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_005159.5(ACTC1):c.717G>A (p.Glu239=)	rs369019849	0.00006
NM_005159.5(ACTC1):c.93T>C (p.Ala31=)	rs1341945129	0.00001
NM_005159.4(ACTC1):c.*1262G>C	rs189725849
NM_005159.4(ACTC1):c.*1732G>C	rs750495564
NM_005159.4(ACTC1):c.*214G>A	rs540240407
NM_005159.5(ACTC1):c.75C>G (p.Gly25=)	rs144819872
NM_005159.5(ACTC1):c.894C>T (p.Asn298=)	rs863225303

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