List of variants in gene TMEM216 reported as likely benign for Meckel syndrome

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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_001173990.3(TMEM216):c.*444T>C	rs116047887	0.02253
NM_001173990.3(TMEM216):c.-24C>G	rs59493015
NM_001173990.3(TMEM216):c.253C>A (p.Arg85=)	rs11230683
NM_001173990.3(TMEM216):c.34+18_34+21del	rs940443692

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