ClinVar Miner

List of variants in gene CTDP1 reported as likely benign for Congenital cataracts-facial dysmorphism-neuropathy syndrome

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_004715.5(CTDP1):c.2070C>T (p.Gly690=)	rs145726709	0.00262
NM_004715.5(CTDP1):c.2649G>A (p.Glu883=)	rs2086667654

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