List of variants in gene combination MDH1, WDPCP studied 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
		ClinVar version:

Total variants: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_005917.4(MDH1):c.3+346A>G	rs201758772	0.00149
NM_005917.4(MDH1):c.208G>A (p.Ala70Thr)	rs533261577	0.00031
NM_005917.4(MDH1):c.200-5C>A	rs78810459	0.00030
NM_005917.4(MDH1):c.858C>T (p.Tyr286=)	rs774885809	0.00020
NM_005917.4(MDH1):c.357C>T (p.Tyr119=)	rs200076644	0.00019
NM_005917.4(MDH1):c.-3A>G	rs201441090	0.00016
NM_005917.4(MDH1):c.225C>T (p.Asp75=)	rs748664587	0.00001
NM_005917.4(MDH1):c.114T>C (p.Leu38=)	rs2468606865
NM_005917.4(MDH1):c.197A>G (p.Lys66Arg)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.