ClinVar Miner

List of variants in gene PLEKHG2 reported as benign 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_022835.3(PLEKHG2):c.2308G>A (p.Ala770Thr)	rs111487768	0.00638
NM_022835.3(PLEKHG2):c.403G>A (p.Gly135Ser)	rs147871368	0.00383

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