ClinVar Miner

List of variants in gene SMC1A reported as benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
HGVS dbSNP
NM_001281463.1(SMC1A):c.*1239T>C rs782502306
NM_001281463.1(SMC1A):c.*2423G>A rs147324052
NM_001281463.1(SMC1A):c.*2856A>T rs148128199
NM_001281463.1(SMC1A):c.*3421G>T rs41304780
NM_001281463.1(SMC1A):c.*3851A>T rs782817464
NM_001281463.1(SMC1A):c.*5016T>C rs17002602
NM_001281463.1(SMC1A):c.*5444G>A rs181871602
NM_001281463.1(SMC1A):c.*5481G>A rs147896900
NM_001281463.1(SMC1A):c.-231C>T rs1264011
NM_001281463.1(SMC1A):c.1107G>A (p.Gln369=) rs147952638
NM_001281463.1(SMC1A):c.1188+11G>C rs144354524
NM_001281463.1(SMC1A):c.1632G>A (p.Glu544=) rs7052858
NM_001281463.1(SMC1A):c.3384C>T (p.Ala1128=) rs142611198
NM_001281463.1(SMC1A):c.346-10C>T rs149219651
NM_006306.4(SMC1A):c.*1542T>C
NM_006306.4(SMC1A):c.*2389G>T
NM_006306.4(SMC1A):c.*4887T>C
NM_006306.4(SMC1A):c.*931A>G

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.