List of variants in gene MTHFR reported as uncertain significance for Thrombophilia due to thrombin defect

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.665C>T (p.Ala222Val)	rs1801133	0.27446
NM_005957.5(MTHFR):c.700G>A (p.Asp234Asn)	rs45589033	0.00004
NM_005957.5(MTHFR):c.1537T>A (p.Leu513Ile)

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