List of variants in gene MTHFR reported as likely pathogenic by Genomic Research Center, Shahid Beheshti University of Medical Sciences

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.1163G>A (p.Arg388His)	rs769953411	0.00002
NM_005957.5(MTHFR):c.379C>T (p.His127Tyr)	rs769381688	0.00001
NM_005957.5(MTHFR):c.237G>T (p.Arg79Ser)	rs1553187509

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