List of variants in gene TMEM126B reported as uncertain significance by GeneDx

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_018480.7(TMEM126B):c.32A>C (p.Lys11Thr)	rs573475998	0.00006
NM_018480.7(TMEM126B):c.466C>A (p.Pro156Thr)	rs145769491	0.00004
NM_018480.7(TMEM126B):c.440T>C (p.Ile147Thr)	rs375039927	0.00003
NM_018480.7(TMEM126B):c.412G>A (p.Glu138Lys)	rs918262592	0.00001
NM_018480.7(TMEM126B):c.204-3T>A
NM_018480.7(TMEM126B):c.227C>T (p.Ala76Val)
NM_018480.7(TMEM126B):c.307G>A (p.Ala103Thr)	rs2082356915
NM_018480.7(TMEM126B):c.463T>C (p.Tyr155His)	rs756088017
NM_018480.7(TMEM126B):c.664A>C (p.Thr222Pro)	rs2547847248

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