ClinVar Miner

List of variants in gene combination POLG, POLGARF reported by Undiagnosed Diseases Network, NIH

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002693.3(POLG):c.391T>C (p.Tyr131His)	rs562847013	0.00027
NM_002693.3(POLG):c.3218C>T (p.Pro1073Leu)	rs267606959	0.00002
NM_002693.3(POLG):c.641C>T (p.Ala214Val)	rs948866053

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