ClinVar Miner

List of variants in gene combination MAK16, TTI2 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001102401.4(TTI2):c.1274T>G (p.Leu425Arg)	rs3736497	0.00027
NM_001102401.4(TTI2):c.1397A>C (p.Asp466Ala)	rs2128826581

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