ClinVar Miner

List of variants in gene OTX2 reported as likely benign for syndromic microphthalmia type 5

Included ClinVar conditions (2):

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_021728.4(OTX2):c.459C>T (p.Ser153=)	rs34537598	0.00961
NM_021728.4(OTX2):c.641C>A (p.Thr214Asn)	rs150982073	0.00013

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