List of variants in gene combination LOC105371520, TMEM107 reported as benign for Meckel syndrome

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_183065.4(TMEM107):c.256+46C>G	rs8064449	0.61047
NM_183065.4(TMEM107):c.87+22A>C	rs78413898	0.01477

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