List of variants reported as likely benign for inborn disorder of serine family metabolism by Mendelics

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_004577.4(PSPH):c.650T>C (p.Val217Ala)	rs73343752	0.00788
NM_000481.4(AMT):c.631G>A (p.Glu211Lys)	rs116192290	0.00735
NM_000170.3(GLDC):c.2316-6dup	rs3215923
NM_004577.4(PSPH):c.95A>G (p.Asp32Gly)	rs78599516

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