List of variants in gene MTHFR reported as likely pathogenic by Department of Pathology and Laboratory Medicine, Sinai Health System

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005957.5(MTHFR):c.1004G>A (p.Arg335His)	rs543016186	0.00005
NM_005957.5(MTHFR):c.1070G>A (p.Arg357His)	rs977038830	0.00001
NM_005957.5(MTHFR):c.469C>T (p.Arg157Trp)	rs776195746	0.00001

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