ClinVar Miner

List of variants in gene combination MTHFS, ST20-MTHFS reported as likely pathogenic by Undiagnosed Diseases Network, NIH

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_006441.4(MTHFS):c.484C>T (p.Gln162Ter)	rs771379232	0.00004
NM_006441.4(MTHFS):c.434G>A (p.Arg145Gln)	rs753635972	0.00002

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