List of variants in gene MTHFR reported as likely benign for not specified

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_005957.5(MTHFR):c.1286A>C (p.Glu429Ala)	rs1801131	0.25830
NM_005957.5(MTHFR):c.236+3A>G	rs1413355	0.00233
NM_005957.5(MTHFR):c.667G>A (p.Asp223Asn)	rs150847674	0.00068
NM_005957.5(MTHFR):c.1167-5G>T	rs1553185653
NM_005957.5(MTHFR):c.1725G>A (p.Val575=)

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