List of variants in gene combination MIR6766, POLG reported as likely benign for Progressive sclerosing poliodystrophy

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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: 14

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HGVS	dbSNP	gnomAD frequency
NM_002693.3(POLG):c.1586-11C>G	rs776821667	0.00007
NM_002693.3(POLG):c.1586-5C>T	rs747270023	0.00004
NM_002693.3(POLG):c.1586-10A>G	rs1060504038	0.00001
NM_002693.3(POLG):c.1586-20G>A	rs768707883	0.00001
NM_002693.3(POLG):c.1586-10A>C
NM_002693.3(POLG):c.1586-11C>A	rs776821667
NM_002693.3(POLG):c.1586-11C>T
NM_002693.3(POLG):c.1586-14C>T
NM_002693.3(POLG):c.1586-16T>C
NM_002693.3(POLG):c.1586-18C>T
NM_002693.3(POLG):c.1586-5C>G
NM_002693.3(POLG):c.1586-6T>A
NM_002693.3(POLG):c.1586-8C>A
NM_002693.3(POLG):c.1586-9C>T

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