List of variants in gene DIAPH1 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_005219.5(DIAPH1):c.117+14C>T	rs2074913	0.05773
NM_005219.5(DIAPH1):c.390C>T (p.Tyr130=)	rs34296458	0.03749
NM_005219.5(DIAPH1):c.3579C>T (p.Gly1193=)	rs2302102	0.02275
NM_005219.5(DIAPH1):c.3765G>A (p.Glu1255=)	rs35755269	0.00955
NM_005219.5(DIAPH1):c.3227T>G (p.Phe1076Cys)	rs143763573	0.00356
NM_005219.5(DIAPH1):c.891G>A (p.Pro297=)	rs116463365	0.00354
NM_005219.5(DIAPH1):c.1407T>C (p.Ile469=)	rs75860159	0.00222
NM_005219.5(DIAPH1):c.1985G>A (p.Gly662Asp)	rs200735096	0.00207
NM_005219.5(DIAPH1):c.1423G>A (p.Glu475Lys)	rs193036129	0.00123
NM_005219.5(DIAPH1):c.2525A>C (p.Gln842Pro)	rs200220260	0.00001
NM_005219.5(DIAPH1):c.1523A>G (p.Asp508Gly)	rs373413837
NM_005219.5(DIAPH1):c.1821TCC[10] (p.Pro620del)	rs3075570
NM_005219.5(DIAPH1):c.1821TCC[12] (p.Pro620dup)	rs3075570
NM_005219.5(DIAPH1):c.1821TCC[13] (p.Pro619_Pro620dup)	rs3075570
NM_005219.5(DIAPH1):c.1821TCC[9] (p.Pro619_Pro620del)	rs3075570
NM_005219.5(DIAPH1):c.402+12del	rs555848272

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