List of variants in gene combination LOC130061785, TMC6 reported as uncertain significance for immune system disorder

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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_001127198.5(TMC6):c.1214G>A (p.Arg405His)	rs149023121	0.00090
NM_001127198.5(TMC6):c.1213C>T (p.Arg405Cys)	rs369868982	0.00007
NM_001127198.5(TMC6):c.1193G>A (p.Arg398His)	rs150505551	0.00004
NM_001127198.5(TMC6):c.1219C>T (p.Arg407Trp)	rs368793235	0.00001

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