ClinVar Miner

List of variants in gene TTC8 reported as likely pathogenic for Retinitis pigmentosa 51; Bardet-Biedl syndrome 8

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_144596.4(TTC8):c.265+1_265+2del	rs1595939517

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