List of variants in gene ATL3 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_015459.5(ATL3):c.580C>T (p.Arg194Cys)	rs372986534	0.00015
NM_015459.5(ATL3):c.1370C>T (p.Ala457Val)	rs746731806	0.00002
NM_015459.5(ATL3):c.138G>C (p.Leu46Phe)	rs372869718	0.00001
NM_015459.5(ATL3):c.1065del (p.Ala356fs)	rs1555051462
NM_015459.5(ATL3):c.14A>G (p.Gln5Arg)
NM_015459.5(ATL3):c.806G>C (p.Gly269Ala)	rs1379629984

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