Condition: Lumbar hyperlordosis
rs864309488
in
GMNN
gene and
Lumbar hyperlordosis
PMID 26637980
2015 De Novo GMNN Mutations Cause Autosomal-Dominant Primordial Dwarfism Associated with Meier-Gorlin Syndrome.
rs878853220
in
LMNA
gene and
Lumbar hyperlordosis
PMID 27717888
2016 New intronic splicing mutation in the LMNA gene causing progressive cardiac conduction defects and variable myopathy.