List of variants in gene LOC105371520, TMEM107 studied 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
		ClinVar version:

Total variants: 5

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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
NM_183065.4(TMEM107):c.256+1G>A	rs1131692180
NM_183065.4(TMEM107):c.295TTC[1] (p.Phe100del)	rs752171066
NM_183065.4(TMEM107):c.384del (p.Leu128fs)	rs1555525895

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