List of variants in gene RAG2 reported as pathogenic 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: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000536.4(RAG2):c.1352G>C (p.Gly451Ala)	rs121918575	0.00004
NM_000536.4(RAG2):c.283G>A (p.Gly95Arg)	rs36001797	0.00003
NM_000536.4(RAG2):c.442C>T (p.Arg148Ter)	rs1315729938	0.00001
NM_000536.4(RAG2):c.104G>C (p.Gly35Ala)	rs148508754
NM_000536.4(RAG2):c.193G>T (p.Asp65Tyr)	rs909264507
NM_000536.4(RAG2):c.2T>C (p.Met1Thr)	rs1554947410
NM_000536.4(RAG2):c.829dup (p.Tyr277fs)	rs1851074524
NM_000536.4(RAG2):c.955G>T (p.Gly319Ter)	rs879541124

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.