Variant: rs1462161137 

    present in Gene: METTL23
    present in Chromosome: 17
    Position on Chromosome: 76733042
    Alleles of this Variant: -/A

rs1462161137 in METTL23 gene and Dysmorphic features PMID 24626631 2014 Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability.

PMID 24501276 2014 METTL23, a transcriptional partner of GABPA, is essential for human cognition.

rs1462161137 in METTL23 gene and Multiple congenital anomalies PMID 24626631 2014 Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability.

PMID 24501276 2014 METTL23, a transcriptional partner of GABPA, is essential for human cognition.

rs1462161137 in METTL23 gene and Muscle hypotonia PMID 24626631 2014 Disruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disability.

PMID 24501276 2014 METTL23, a transcriptional partner of GABPA, is essential for human cognition.