ClinVar Miner

List of variants in gene TULP1 reported as benign for GUCY2D retinopathy

Included ClinVar conditions (13):

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_003322.6(TULP1):c.783G>C (p.Lys261Asn)	rs2064318	0.84569
NM_003322.6(TULP1):c.776T>C (p.Ile259Thr)	rs2064317	0.36637

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