List of variants in gene CEP152 reported as uncertain significance for not specified

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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: 26

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HGVS	dbSNP	gnomAD frequency
NM_001194998.2(CEP152):c.3839A>G (p.Asp1280Gly)	rs539483307	0.00028
NM_001194998.2(CEP152):c.4603G>A (p.Val1535Ile)	rs372654467	0.00024
NM_001194998.2(CEP152):c.186C>T (p.Asp62=)	rs548567364	0.00016
NM_001194998.2(CEP152):c.2751G>A (p.Met917Ile)	rs189636635	0.00014
NM_001194998.2(CEP152):c.685A>C (p.Asn229His)	rs147595936	0.00013
NM_001194998.2(CEP152):c.3934C>T (p.Arg1312Cys)	rs751031882	0.00005
NM_001194998.2(CEP152):c.1862T>C (p.Ile621Thr)	rs372860195	0.00004
NM_001194998.2(CEP152):c.1116G>C (p.Glu372Asp)	rs369383335	0.00003
NM_001194998.2(CEP152):c.2090A>G (p.His697Arg)	rs774173743	0.00003
NM_001194998.2(CEP152):c.4702C>A (p.Leu1568Ile)	rs777337799	0.00003
NM_001194998.2(CEP152):c.2148-17G>A	rs751691427	0.00002
NM_001194998.2(CEP152):c.4094-1G>A	rs759175035	0.00002
NM_001194998.2(CEP152):c.4292T>C (p.Ile1431Thr)	rs375113825	0.00002
NM_001194998.2(CEP152):c.540+6G>A	rs770422442	0.00002
NM_001194998.2(CEP152):c.60C>T (p.Asp20=)	rs759826252	0.00002
NM_001194998.2(CEP152):c.1008G>A (p.Leu336=)	rs1896842918	0.00001
NM_001194998.2(CEP152):c.5087G>A (p.Ser1696Asn)	rs1892706413	0.00001
NM_001194998.2(CEP152):c.1549G>C (p.Val517Leu)	rs1555424276
NM_001194998.2(CEP152):c.1577+3A>G	rs1196921831
NM_001194998.2(CEP152):c.3071G>T (p.Arg1024Leu)	rs199914670
NM_001194998.2(CEP152):c.4213A>G (p.Thr1405Ala)	rs2140546380
NM_001194998.2(CEP152):c.4365_4376delinsGTT (p.Ser1455_Asn1459delinsArgPhe)	rs797045455
NM_001194998.2(CEP152):c.4433A>T (p.Lys1478Met)	rs2140543971
NM_001194998.2(CEP152):c.5128G>A (p.Asp1710Asn)	rs1892703145
NM_001194998.2(CEP152):c.87+26_87+27del	rs372967874
NM_001194998.2(CEP152):c.87+9dup	rs1555429164

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