List of variants in gene TSPAN10 reported as likely benign

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001290212.2(TSPAN10):c.598C>T (p.Arg200Cys)	rs368751739	0.00005
NM_001290212.2(TSPAN10):c.397G>A (p.Ala133Thr)
NM_001290212.2(TSPAN10):c.790C>G (p.Arg264Gly)

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