List of variants in gene GGCX reported as likely benign by Illumina Laboratory Services, Illumina

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: 19

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000821.7(GGCX):c.*3447del	rs71390078	0.11046
NM_000821.7(GGCX):c.3370_3372del	rs200418394	0.02987
NM_000821.7(GGCX):c.*781A>C	rs142680507	0.01337
NM_000821.7(GGCX):c.*962G>C	rs78372899	0.00425
NM_000821.7(GGCX):c.*1277G>A	rs60864851	0.00397
NM_000821.7(GGCX):c.189C>T (p.Ser63=)	rs41290035	0.00277
NM_000821.7(GGCX):c.582C>T (p.His194=)	rs76767923	0.00271
NM_000821.7(GGCX):c.*463G>A	rs553383801	0.00149
NM_000821.7(GGCX):c.*3067T>C	rs139304933	0.00090
NM_000821.7(GGCX):c.*680G>C	rs139300235	0.00090
NM_000821.7(GGCX):c.*1916C>T	rs192730155	0.00069
NM_000821.7(GGCX):c.15C>T (p.Ala5=)	rs199867398	0.00018
NM_000821.7(GGCX):c.*165A>G	rs181695165	0.00007
NM_000821.7(GGCX):c.*2822C>T	rs190959810	0.00007
NM_000821.7(GGCX):c.*2811T>C	rs118153916	0.00006
NM_000821.7(GGCX):c.1378G>A (p.Val460Ile)	rs149078813	0.00006
NM_000821.7(GGCX):c.*4314T>C	rs530247310	0.00001
NM_000821.7(GGCX):c.*1282G>A	rs574843893
NM_000821.7(GGCX):c.1889-17_1889-16del	rs528396383

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.