List of variants in gene TIMM44 reported as likely benign by Mayo Clinic Laboratories, Mayo Clinic

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_006351.4(TIMM44):c.1114A>G (p.Ile372Val)	rs11542187	0.03146
NM_006351.4(TIMM44):c.753C>G (p.Asn251Lys)	rs118048213	0.02472
NM_006351.4(TIMM44):c.184G>A (p.Gly62Ser)	rs144317041	0.00890
NM_006351.4(TIMM44):c.69A>G (p.Gln23=)	rs35992331	0.00532
NM_006351.4(TIMM44):c.138A>G (p.Pro46=)	rs145509783	0.00316

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