List of variants in gene combination AMPD2, LOC126805822 reported as likely benign for Pontocerebellar hypoplasia type 9

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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_001368809.2(AMPD2):c.1587C>A (p.Thr529=)	rs35337955	0.00159
NM_001368809.2(AMPD2):c.1699-11T>C	rs188035528	0.00087
NM_001368809.2(AMPD2):c.1326T>C (p.Pro442=)	rs371970036	0.00024

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