ClinVar Miner

List of variants in gene TMEM126B reported as likely pathogenic by Revvity Omics, Revvity

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_018480.7(TMEM126B):c.635G>T (p.Gly212Val)	rs141542003	0.00103
NM_018480.7(TMEM126B):c.320_321del (p.Tyr107fs)	rs752316853

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