List of variants in gene combination FANCI, POLG studied for Hereditary spastic paraplegia

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_002693.3(POLG):c.3708G>T (p.Gln1236His)	rs3087374	0.06023
NM_002693.3(POLG):c.2958C>T (p.Tyr986=)	rs2307431	0.02985
NM_002693.3(POLG):c.3428A>G (p.Glu1143Gly)	rs2307441	0.02704
NM_002693.3(POLG):c.3667A>G (p.Ile1223Val)	rs148786642	0.00004

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