List of variants in gene MDH2 reported as pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_005918.4(MDH2):c.398C>T (p.Pro133Leu)	rs375002796	0.00003
NM_005918.4(MDH2):c.429+1G>T	rs782251807	0.00001
NM_005918.4(MDH2):c.157dup (p.Leu53fs)	rs782759642
NM_005918.4(MDH2):c.167_168del (p.Leu55_Tyr56insTer)	rs782494815
NM_005918.4(MDH2):c.205dup (p.Ser69fs)
NM_005918.4(MDH2):c.489del (p.Asn164fs)
NM_005918.4(MDH2):c.543del (p.Ala182fs)
NM_005918.4(MDH2):c.591del (p.Ile197fs)	rs2116696690

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