List of variants in gene MTHFD1 reported as likely pathogenic for not provided

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_005956.4(MTHFD1):c.298C>T (p.Gln100Ter)	rs1329424461	0.00001
NM_005956.4(MTHFD1):c.727+1G>A	rs781065280	0.00001
NM_005956.4(MTHFD1):c.953+1G>A	rs778570054	0.00001
NM_005956.4(MTHFD1):c.1090_1127+63del
NM_005956.4(MTHFD1):c.1264+1G>A
NM_005956.4(MTHFD1):c.1494+1G>A
NM_005956.4(MTHFD1):c.1494+1G>C
NM_005956.4(MTHFD1):c.1996+1G>A
NM_005956.4(MTHFD1):c.241-4_250del
NM_005956.4(MTHFD1):c.615+1G>A

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