List of variants in gene PPP1CB reported as benign for not provided

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: 18

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002709.3(PPP1CB):c.201A>G (p.Gln67=)	rs1128416	0.57257
NM_002709.3(PPP1CB):c.521-182G>C	rs6547877	0.57250
NM_002709.3(PPP1CB):c.416-305T>C	rs6730321	0.41421
NM_002709.3(PPP1CB):c.521-257G>A	rs60287247	0.05279
NM_002709.3(PPP1CB):c.415+86A>C	rs17743079	0.04625
NM_002709.3(PPP1CB):c.52+15G>T	rs113766757	0.00563
NM_002709.3(PPP1CB):c.416-17A>G	rs6727624	0.00279
NM_002709.3(PPP1CB):c.53-9G>A	rs368197884	0.00172
NM_002709.3(PPP1CB):c.27C>T (p.Asp9=)	rs141050112	0.00136
NM_002709.3(PPP1CB):c.520+7T>C	rs200836202	0.00036
NM_002709.2(PPP1CB):c.-308G>A	rs377326423
NM_002709.2(PPP1CB):c.-325G>A	rs766627964
NM_002709.3(PPP1CB):c.52+65G>C	rs2276547
NM_002709.3(PPP1CB):c.520+215G>A	rs6740859
NM_002709.3(PPP1CB):c.520+36dup
NM_002709.3(PPP1CB):c.521-138dup	rs11449670
NM_002709.3(PPP1CB):c.593-184_593-181del	rs5830089
NM_002709.3(PPP1CB):c.880-246del	rs5830090

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.