List of variants in gene TMEM231 reported as uncertain significance for Meckel syndrome, type 11

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001077418.3(TMEM231):c.119T>G (p.Leu40Arg)	rs1567441193
NM_001077418.3(TMEM231):c.526C>G (p.Leu176Val)	rs775613602
NM_001077418.3(TMEM231):c.771-5_771-2delinsTGTC	rs2080606129

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