List of variants in gene CETN3 reported as uncertain significance

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_004365.4(CETN3):c.171G>C (p.Leu57Phe)	rs1432934573	0.00001
NM_004365.4(CETN3):c.196G>A (p.Val66Ile)	rs1749422001	0.00001
NM_004365.4(CETN3):c.322A>C (p.Lys108Gln)	rs1286811424	0.00001
NM_004365.4(CETN3):c.332A>G (p.Asp111Gly)	rs765211712	0.00001
NM_004365.4(CETN3):c.400A>T (p.Met134Leu)	rs1284047263	0.00001
NM_004365.4(CETN3):c.118G>A (p.Asp40Asn)
NM_004365.4(CETN3):c.226G>A (p.Glu76Lys)	rs778660472
NM_004365.4(CETN3):c.229G>C (p.Ala77Pro)	rs1373346470
NM_004365.4(CETN3):c.230C>T (p.Ala77Val)
NM_004365.4(CETN3):c.434A>G (p.Glu145Gly)	rs2531470282
NM_004365.4(CETN3):c.88A>G (p.Ile30Val)

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