List of variants in gene MTHFR reported as pathogenic for blood coagulation disease

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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.155G>A (p.Arg52Gln)	rs754980119	0.00004
NM_005957.5(MTHFR):c.1632+2T>G	rs749765738	0.00001
NM_005957.5(MTHFR):c.202C>G (p.Arg68Gly)	rs763539350	0.00001
NM_005957.5(MTHFR):c.548G>A (p.Arg183Gln)	rs574132670	0.00001
NM_005957.5(MTHFR):c.680C>T (p.Thr227Met)	rs748571395	0.00001

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