ClinVar Miner

List of variants in gene DIS3L2 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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_152383.5(DIS3L2):c.301G>T (p.Ala101Ser)	rs199857926	0.00028
NM_152383.5(DIS3L2):c.1430T>G (p.Leu477Arg)	rs201719374	0.00022

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