ClinVar Miner

List of variants in gene combination EIF2B4, GTF3C2 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_001034116.2(EIF2B4):c.961C>T (p.Arg321Cys)	rs200954953	0.00010
NM_001034116.2(EIF2B4):c.1052C>T (p.Thr351Ile)	rs779707712	0.00001

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