Variant: rs1057519074 

    present in Gene: MSN
    present in Chromosome: X
    Position on Chromosome: 65731150
    Alleles of this Variant: C/T

rs1057519074 in MSN gene and IMMUNODEFICIENCY 50 PMID 28378256 2017 First Case of X-Linked Moesin Deficiency Identified After Newborn Screening for SCID.

PMID 27405666 2016 X-linked primary immunodeficiency associated with hemizygous mutations in the moesin (MSN) gene.

PMID 29556235 2018 Exome Sequencing Diagnoses X-Linked Moesin-Associated Immunodeficiency in a Primary Immunodeficiency Case.