ClinVar Miner

List of variants in gene LMNA reported as uncertain significance for Congenital muscular dystrophy, LMNA-related

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
HGVS dbSNP
NM_005572.3(LMNA):c.*103C>T rs1057516022
NM_005572.3(LMNA):c.-109G>T rs886045360
NM_005572.3(LMNA):c.-138T>C rs886045359
NM_005572.3(LMNA):c.-142C>A rs886045358
NM_005572.3(LMNA):c.-183C>A rs886045357
NM_005572.3(LMNA):c.-210T>C rs886045356
NM_005572.3(LMNA):c.-225C>A rs886045355
NM_005572.3(LMNA):c.-226C>T rs886045354
NM_005572.3(LMNA):c.-5C>A rs886045362
NM_005572.3(LMNA):c.-62C>A rs886045361
NM_005572.3(LMNA):c.113T>A (p.Leu38His)
NM_005572.3(LMNA):c.1391T>A (p.Met464Lys)
NM_005572.3(LMNA):c.294G>A (p.Glu98=) rs886045363
NM_005572.3(LMNA):c.295C>A (p.Arg99Ser) rs886045364
NM_005572.3(LMNA):c.514-11C>T rs886045365
NM_005572.3(LMNA):c.936+12C>T rs199881992
NM_005572.3(LMNA):c.985C>A (p.Arg329Ser) rs775159300
NM_170707.3(LMNA):c.703C>A (p.Arg235Ser)

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.