List of variants in gene MTHFR reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_005957.5(MTHFR):c.*174del	rs776554158	0.00121
NM_005957.5(MTHFR):c.367_369dup	rs886045191	0.00001
NM_005957.5(MTHFR):c.*1018A>G	rs886045187
NM_005957.5(MTHFR):c.372_373insTACC	rs886045190
NM_005957.5(MTHFR):c.*702del	rs775036001
NM_005957.5(MTHFR):c.-69_-63del	rs886045194
NM_005957.5(MTHFR):c.1753-14dup	rs758514539
NM_005957.5(MTHFR):c.277G>A (p.Val93Met)

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