List of variants in gene MTHFR reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

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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.1286A>C (p.Glu429Ala)	rs1801131	0.25830
NM_005957.5(MTHFR):c.1129C>T (p.Arg377Cys)	rs121434296	0.00004
NM_005957.5(MTHFR):c.1699C>T (p.Arg567Ter)	rs140277700	0.00003
NM_005957.5(MTHFR):c.1743G>A (p.Met581Ile)	rs45590836	0.00003
NM_005957.5(MTHFR):c.470G>A (p.Arg157Gln)	rs121434295	0.00002
NM_005957.5(MTHFR):c.1072C>T (p.Arg358Ter)	rs377443637	0.00001
NM_005957.5(MTHFR):c.968T>C (p.Leu323Pro)	rs121434297	0.00001
MTHFR, 1081C-T
NM_005957.5(MTHFR):c.1015T>G (p.Trp339Gly)	rs267606886
NM_005957.5(MTHFR):c.547C>T (p.Arg183Ter)	rs121434294
NM_005957.5(MTHFR):c.971A>G (p.Asn324Ser)	rs267606887

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