ClinVar Miner

List of variants in gene NBN reported as likely benign by PreventionGenetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
NM_002485.4(NBN):c.1089C>T (p.Tyr363=) rs121908974
NM_002485.4(NBN):c.1124+6G>T rs375862750
NM_002485.4(NBN):c.1419A>G (p.Gln473=) rs587780535
NM_002485.4(NBN):c.171+4T>C rs587782290
NM_002485.4(NBN):c.1720T>A (p.Leu574Ile) rs142334798
NM_002485.4(NBN):c.1890A>C (p.Ser630=) rs587780778
NM_002485.4(NBN):c.1914+10G>A rs577706448
NM_002485.4(NBN):c.2234+16C>T rs1563497498
NM_002485.4(NBN):c.2235-18C>T rs138106214
NM_002485.4(NBN):c.283G>A (p.Asp95Asn) rs61753720
NM_002485.4(NBN):c.38-19A>T rs766849651
NM_002485.4(NBN):c.453C>T (p.Val151=) rs1176879721
NM_002485.4(NBN):c.702+9G>A rs748373099
NM_002485.4(NBN):c.703-14C>T rs1411178267
NM_002485.4(NBN):c.939G>A (p.Ala313=) rs145750430

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.