List of variants in gene MTHFR reported as likely benign for hematologic disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_005957.5(MTHFR):c.1959G>A (p.Thr653=)	rs45572531	0.00187
NM_005957.5(MTHFR):c.1409A>T (p.Glu470Val)	rs142617551	0.00183
NM_005957.5(MTHFR):c.1555C>T (p.Arg519Cys)	rs45496998	0.00176
NM_005957.5(MTHFR):c.1371T>C (p.Asp457=)	rs1428673436	0.00001

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