ClinVar Miner

List of variants in gene ROBO2 reported as benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
NM_001128929.3(ROBO2):c.*1114G>A rs11127602
NM_001128929.3(ROBO2):c.*1216C>T rs1031377
NM_001128929.3(ROBO2):c.*2196G>A rs117129934
NM_001128929.3(ROBO2):c.*2737G>A rs1163748
NM_001128929.3(ROBO2):c.*3001A>G rs114795420
NM_001128929.3(ROBO2):c.*3236G>A rs1163750
NM_001128929.3(ROBO2):c.*3923C>T rs10865561
NM_001128929.3(ROBO2):c.110-14G>T rs61731268
NM_001128929.3(ROBO2):c.110-57466T>G rs3923744
NM_001128929.3(ROBO2):c.110-57632G>C rs79942150
NM_001128929.3(ROBO2):c.110-57770T>C rs3923745
NM_001128929.3(ROBO2):c.142C>A (p.Arg48=) rs6788280
NM_001128929.3(ROBO2):c.1592A>T (p.Asn531Ile) rs80051448
NM_001128929.3(ROBO2):c.19C>A (p.Arg7Ser) rs12171318
NM_001128929.3(ROBO2):c.3602+13del rs78824327
NM_001128929.3(ROBO2):c.73G>A (p.Val25Met) rs78834776

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.