List of variants in gene CHCHD10 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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_213720.3(CHCHD10):c.100C>T (p.Pro34Ser)	rs551521196	0.00237
NM_213720.3(CHCHD10):c.239C>T (p.Pro80Leu)	rs775332895	0.00016
NM_213720.3(CHCHD10):c.378C>T (p.Ser126=)	rs199579266	0.00012
NM_213720.3(CHCHD10):c.171G>A (p.Val57=)	rs780298646	0.00007
NM_213720.3(CHCHD10):c.189C>T (p.His63=)	rs202148090	0.00001
NM_213720.3(CHCHD10):c.69G>C (p.Pro23=)

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