Variant: rs114638163 

    present in Gene: MIPEP
    present in Chromosome: 13
    Position on Chromosome: 23805994
    Alleles of this Variant: C/A;T

rs114638163 in MIPEP gene and Cardiomyopathies PMID 27799064 2016 MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.

rs114638163 in MIPEP gene and Cardiomyopathy, Dilated PMID 27799064 2016 MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.

rs114638163 in MIPEP gene and Congenital cataract PMID 27799064 2016 MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.

rs114638163 in MIPEP gene and Generalized hypotonia PMID 27799064 2016 MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.

rs114638163 in MIPEP gene and Global developmental delay PMID 27799064 2016 MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.

rs114638163 in MIPEP gene and Infantile muscular hypotonia PMID 27799064 2016 MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.

rs114638163 in MIPEP gene and Left ventricular noncompaction PMID 27799064 2016 MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.

rs114638163 in MIPEP gene and Left ventricular noncompaction cardiomyopathy PMID 27799064 2016 MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.

rs114638163 in MIPEP gene and Seizures PMID 27799064 2016 MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.