List of variants in gene combination TNFSF12, TNFSF12-TNFSF13 reported as benign for Common variable immunodeficiency

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

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003809.3(TNFSF12):c.600G>C (p.Ala200=)	rs3803798	0.50487
NM_003809.3(TNFSF12):c.276C>A (p.Arg92=)	rs62059804	0.20757
NM_003809.3(TNFSF12):c.642G>T (p.Gly214=)	rs4968189	0.01736
NM_003809.3(TNFSF12):c.338-9A>G	rs114577645	0.01655
NM_003809.3(TNFSF12):c.597G>A (p.Ala199=)	rs143039184	0.00141
NM_003809.3(TNFSF12):c.609C>T (p.Leu203=)	rs140608168	0.00140
NM_003809.3(TNFSF12):c.160-19G>A	rs137994694	0.00069
NM_003809.3(TNFSF12):c.429T>G (p.Pro143=)	rs770924960	0.00012
NM_003809.3(TNFSF12):c.204G>A (p.Pro68=)	rs751381442	0.00005
NM_003809.3(TNFSF12):c.499-8del
NM_003809.3(TNFSF12):c.642= (p.Gly214=)

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.