ClinVar Miner

List of variants reported as benign for anterior segment dysgenesis 1

Included ClinVar conditions (3):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005029.4(PITX3):c.285C>T (p.Ile95=)	rs2281983	0.66644
NM_000325.6(PITX2):c.*454C>T	rs6533526	0.05143
NM_012186.3(FOXE3):c.146G>C (p.Gly49Ala)	rs566961335	0.01396

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