List of variants in gene combination LOC130059440, TMEM231 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001077418.3(TMEM231):c.140-15C>T	rs201518524	0.00019
NM_001077418.3(TMEM231):c.140-35C>T	rs750621210	0.00002
NM_001077418.3(TMEM231):c.140-29C>T
NM_001077418.3(TMEM231):c.140-2A>G	rs1216670609
NM_001077418.3(TMEM231):c.140-47C>G	rs369232571
NM_001077418.3(TMEM231):c.140-5C>T

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