ClinVar Miner

List of variants in gene SMC1A reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 25
Download table as spreadsheet
HGVS dbSNP
NM_001281463.1(SMC1A):c.219C>G (p.Ala73=) rs587784414
NM_001281463.1(SMC1A):c.2722C>T (p.Leu908=) rs781912370
NM_001281463.1(SMC1A):c.3324C>T (p.Gly1108=) rs374246357
NM_006306.4(SMC1A):c.1101G>A (p.Leu367=) rs782695048
NM_006306.4(SMC1A):c.1563C>T (p.Asp521=)
NM_006306.4(SMC1A):c.2059-9T>C rs782041729
NM_006306.4(SMC1A):c.2184C>A (p.Ala728=) rs968499171
NM_006306.4(SMC1A):c.2583G>A (p.Lys861=) rs1602405816
NM_006306.4(SMC1A):c.2643G>A (p.Lys881=) rs1602405773
NM_006306.4(SMC1A):c.2688G>A (p.Lys896=) rs1602405737
NM_006306.4(SMC1A):c.2863-8C>T rs782738954
NM_006306.4(SMC1A):c.2886A>C (p.Ser962=) rs782788248
NM_006306.4(SMC1A):c.2949C>T (p.Tyr983=) rs1390804289
NM_006306.4(SMC1A):c.298+9G>A rs1556891082
NM_006306.4(SMC1A):c.3135T>C (p.Phe1045=) rs1602398671
NM_006306.4(SMC1A):c.3437+10A>T rs782079503
NM_006306.4(SMC1A):c.3615T>A (p.Pro1205=) rs1602397790
NM_006306.4(SMC1A):c.3666G>A (p.Lys1222=) rs1602397606
NM_006306.4(SMC1A):c.372G>C (p.Leu124Phe) rs148835205
NM_006306.4(SMC1A):c.381C>T (p.Leu127=)
NM_006306.4(SMC1A):c.552T>C (p.Phe184=) rs1556890821
NM_006306.4(SMC1A):c.594A>G (p.Glu198=) rs1556890814
NM_006306.4(SMC1A):c.616-7del rs1312306004
NM_006306.4(SMC1A):c.846G>A (p.Lys282=) rs1602413372
NM_006306.4(SMC1A):c.915C>T (p.Thr305=) rs782522248

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.