List of variants in gene MIEF1 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_019008.6(MIEF1):c.911G>A (p.Arg304His)	rs141041315	0.00650
NM_019008.6(MIEF1):c.664G>A (p.Asp222Asn)	rs138446352	0.00216
NM_019008.6(MIEF1):c.1125G>A (p.Pro375=)
NM_019008.6(MIEF1):c.359G>C (p.Arg120Thr)
NM_019008.6(MIEF1):c.505C>T (p.Arg169Trp)

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