List of variants in gene C3orf70 reported as uncertain significance for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001025266.3(C3orf70):c.433T>C (p.Tyr145His)	rs144031288	0.00051
NM_001025266.3(C3orf70):c.5G>A (p.Ser2Asn)	rs374173126	0.00021
NM_001025266.3(C3orf70):c.482A>G (p.Glu161Gly)	rs772679017	0.00003
NM_001025266.3(C3orf70):c.458A>G (p.His153Arg)	rs955820356

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