List of variants in gene MT-CYB reported as likely benign for not provided

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: 11

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.15071T>C	rs199999794
NC_012920.1(MT-CYB):m.15777G>A	rs879182710
NC_012920.1:m.14911C>T	rs28357683
NC_012920.1:m.15191T>C	rs878912989
NC_012920.1:m.15217G>A	rs193302989
NC_012920.1:m.15262T>C	rs1057520097
NC_012920.1:m.15487A>G	rs28357370
NC_012920.1:m.15511T>C	rs527236188
NC_012920.1:m.15514T>C	rs878853086
NC_012920.1:m.15833C>T	rs41504845
m.15497G>A	rs199951903

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