List of variants in gene ANKRD1 reported as likely 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_014391.3(ANKRD1):c.319G>T (p.Val107Leu)	rs114435632	0.00269
NM_014391.3(ANKRD1):c.208-15G>A	rs116511484	0.00184
NM_014391.3(ANKRD1):c.441T>C (p.Asp147=)	rs145827106	0.00018
NM_014391.3(ANKRD1):c.150C>G (p.Ala50=)	rs147484763	0.00006
NM_014391.3(ANKRD1):c.838A>G (p.Ile280Val)	rs144770680	0.00004
NM_014391.3(ANKRD1):c.560C>T (p.Ser187Phe)	rs397517251	0.00001
NM_014391.3(ANKRD1):c.145C>T (p.Leu49=)	rs1554827991
NM_014391.3(ANKRD1):c.154C>T (p.Pro52Ser)	rs397517248
NM_014391.3(ANKRD1):c.346-17_346-10del	rs397517250
NM_014391.3(ANKRD1):c.346-18_346-9del	rs727502890

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