ClinVar Miner

List of variants in gene MTHFR reported as pathogenic by Genetics and Genomic Medicine Centre, NeuroGen Healthcare, NeuroGen Healthcare

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_005957.5(MTHFR):c.459C>G (p.Ile153Met)	rs767890671	0.00005
NM_005957.5(MTHFR):c.1517A>G (p.Tyr506Cys)	rs764650203	0.00001

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