ClinVar Miner

List of variants reported as not provided for POLG-related disorder by GenomeConnect - Invitae Patient Insights Network

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_002693.3(POLG):c.752C>T (p.Thr251Ile)	rs113994094	0.00151
NM_002693.3(POLG):c.2051A>G (p.Asn684Ser)	rs202244328	0.00007

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