List of variants in gene TTLL5 reported as likely pathogenic for cone-rod dystrophy

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
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_015072.5(TTLL5):c.2412_2420delinsAATTTTTT (p.Thr805fs)
NM_015072.5(TTLL5):c.3177_3180del (p.Thr1059_Asn1060insTer)	rs772656461
NM_015072.5(TTLL5):c.987A>T (p.Glu329Asp)	rs1555384338

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