List of variants in gene TIMM44 reported as likely benign by GeneDx

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_006351.4(TIMM44):c.1272G>A (p.Ala424=)	rs138385134	0.00064
NM_006351.4(TIMM44):c.58A>G (p.Ser20Gly)	rs149700042	0.00048
NM_006351.4(TIMM44):c.580G>A (p.Val194Ile)	rs147925283	0.00020
NM_006351.4(TIMM44):c.1038+35del	rs58157552
NM_006351.4(TIMM44):c.313-25_313-23del	rs753419157
NM_006351.4(TIMM44):c.771G>C (p.Arg257=)	rs1057522943

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