List of variants in gene DIAPH3 reported as uncertain significance 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001042517.2(DIAPH3):c.3082G>A (p.Val1028Ile)	rs541616926	0.00004
NM_001042517.2(DIAPH3):c.1205A>C (p.Glu402Ala)
NM_001042517.2(DIAPH3):c.1840C>T (p.Pro614Ser)
NM_001042517.2(DIAPH3):c.2266-2A>G	rs1593949468
NM_001042517.2(DIAPH3):c.2777G>C (p.Gly926Ala)
NM_001042517.2(DIAPH3):c.927del (p.Ala310fs)

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