List of variants in gene PSAT1 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_058179.4(PSAT1):c.296C>T (p.Ala99Val)	rs587777778	0.00019
NM_058179.4(PSAT1):c.870-1G>T	rs376824714	0.00003
NM_058179.4(PSAT1):c.299A>C (p.Asp100Ala)	rs118203967	0.00001

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