List of variants in gene CERS3 reported as benign by GeneDx

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: 35

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HGVS	dbSNP	gnomAD frequency
NM_001378789.1(CERS3):c.1108A>G (p.Arg370Gly)	rs2439928	0.98616
NM_001378789.1(CERS3):c.845+265G>A	rs1966045	0.98479
NM_001378789.1(CERS3):c.846-144C>T	rs2014940	0.98459
NM_001378789.1(CERS3):c.516+104G>A	rs2654574	0.98431
NM_001378789.1(CERS3):c.465+155G>A	rs2654572	0.87780
NM_001378789.1(CERS3):c.288+283C>T	rs2654629	0.87550
NM_001378789.1(CERS3):c.159A>G (p.Arg53=)	rs1354332	0.78557
NM_001378789.1(CERS3):c.173+136G>A	rs2587778	0.77802
NM_001378789.1(CERS3):c.466-136C>A	rs2587763	0.75581
NM_001378789.1(CERS3):c.999+60G>A	rs12595207	0.68951
NM_001378789.1(CERS3):c.999+173T>C	rs12050655	0.49140
NM_001378789.1(CERS3):c.845+109T>A	rs34108242	0.42848
NM_001378789.1(CERS3):c.845+53C>T	rs12909732	0.42838
NM_001378789.1(CERS3):c.845+334G>A	rs12906592	0.42806
NM_001378789.1(CERS3):c.999+21del	rs11323964	0.29599
NM_001378789.1(CERS3):c.465+65A>T	rs2587764	0.22974
NM_001378789.1(CERS3):c.174-306C>T	rs1847323	0.12886
NM_001378789.1(CERS3):c.174-81G>A	rs1503479	0.12839
NM_001378789.1(CERS3):c.466-110G>T	rs12437474	0.11360
NM_001378789.1(CERS3):c.845+202C>T	rs12592478	0.11167
NM_001378789.1(CERS3):c.134A>G (p.Tyr45Cys)	rs60405735	0.11146
NM_001378789.1(CERS3):c.465+129C>G	rs8040737	0.09962
NM_001378789.1(CERS3):c.609+200T>C	rs62038991	0.06307
NM_001378789.1(CERS3):c.407+305A>G	rs2654633	0.05423
NM_001378789.1(CERS3):c.12G>A (p.Thr4=)	rs77089459	0.04634
NM_001378789.1(CERS3):c.738+6C>T	rs1566775	0.04327
NM_001378789.1(CERS3):c.407+74C>T	rs10468191	0.01838
NM_001378789.1(CERS3):c.881A>G (p.His294Arg)	rs114065539	0.00815
NM_001378789.1(CERS3):c.*75C>A	rs1023782
NM_001378789.1(CERS3):c.174-201dup	rs138738369
NM_001378789.1(CERS3):c.407+309del	rs71665897
NM_001378789.1(CERS3):c.465+221_465+222del	rs34347308
NM_001378789.1(CERS3):c.466-181G>C	rs2654573
NM_001378789.1(CERS3):c.738+203C>A	rs73472039
NM_001378789.1(CERS3):c.999+232T>A	rs12592841

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