List of variants in gene MT-CYB reported as uncertain significance by Department of Pediatrics, Division of Medical Genetics, Faculty of Medicine Ramathibodi Hospital, Mahidol University

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: 7

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.16230A>G	rs2853514
NC_012920.1(MT-CYB):m.16274G>A	rs144095641
NC_012920.1(MT-CYB):m.16319G>A	rs35105996
NC_012920.1(MT-CYB):m.235A>G	rs3937037
NC_012920.1(MT-CYB):m.249del	rs879043227
NC_012920.1(MT-CYB):m.515AC[4]	rs78907894
NC_012920.1(MT-CYB):m.8272CCCCCTCTA[1]	rs369704279

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