List of variants in gene MTHFR reported as 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_005957.5(MTHFR):c.1305C>T (p.Phe435=)	rs4846051	0.90843
NM_005957.5(MTHFR):c.1166+31C>T	rs1994798	0.56165
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.1167-76G>T	rs12121543	0.20910
NM_005957.5(MTHFR):c.1056C>T (p.Ser352=)	rs2066462	0.09546
NM_005957.5(MTHFR):c.1305= (p.Phe435=)	rs4846051	0.09157
NM_005957.5(MTHFR):c.117C>T (p.Pro39=)	rs2066470	0.09092
NM_005957.5(MTHFR):c.1781G>A (p.Arg594Gln)	rs2274976	0.04451
NM_005957.5(MTHFR):c.1958C>T (p.Thr653Met)	rs35737219	0.01399
NM_005957.5(MTHFR):c.1476G>A (p.Pro492=)	rs35653697	0.00937
NM_005957.5(MTHFR):c.276C>T (p.Asp92=)	rs45546035	0.00201
NM_005957.5(MTHFR):c.1959G>A (p.Thr653=)	rs45572531	0.00190
NM_005957.5(MTHFR):c.417G>A (p.Thr139=)	rs2066466	0.00106

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