List of variants in gene MFN2 reported by Institute of Human Genetics, University of Leipzig Medical Center

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_014874.4(MFN2):c.2119C>T (p.Arg707Trp)	rs119103267	0.00029
NM_014874.4(MFN2):c.1160+1G>A	rs1553144086
NM_014874.4(MFN2):c.494A>G (p.His165Arg)	rs863224970
NM_014874.4(MFN2):c.695C>G (p.Thr232Ser)	rs1569842764
NM_014874.4(MFN2):c.781G>C (p.Asp261His)	rs2100832682
NM_014874.4(MFN2):c.827A>G (p.Gln276Arg)	rs119103264

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