List of variants in gene TMEM186 reported as likely benign

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_015421.4(TMEM186):c.539G>A (p.Arg180Gln)	rs201350921	0.00003
NM_015421.4(TMEM186):c.204C>T (p.Phe68=)	rs756019804	0.00002
NM_015421.4(TMEM186):c.500C>G (p.Thr167Ser)	rs772054886	0.00001
NM_015421.4(TMEM186):c.200C>T (p.Thr67Ile)
NM_015421.4(TMEM186):c.472A>G (p.Met158Val)

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