Variant: rs1555537637 

    present in Gene: SPNS2
    present in Chromosome: 17
    Position on Chromosome: 4533107
    Alleles of this Variant: CC/T

rs1555537637 in SPNS2 gene and Dysmorphic features PMID 19074308 2009 The sphingolipid transporter spns2 functions in migration of zebrafish myocardial precursors.

PMID 25356849 2014 Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss.

PMID 27899622 2017 UniProt: the universal protein knowledgebase.

rs1555537637 in SPNS2 gene and Multiple congenital anomalies PMID 25356849 2014 Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss.

PMID 27899622 2017 UniProt: the universal protein knowledgebase.

PMID 19074308 2009 The sphingolipid transporter spns2 functions in migration of zebrafish myocardial precursors.

rs1555537637 in SPNS2 gene and Muscle hypotonia PMID 25356849 2014 Spinster homolog 2 (spns2) deficiency causes early onset progressive hearing loss.

PMID 19074308 2009 The sphingolipid transporter spns2 functions in migration of zebrafish myocardial precursors.

PMID 27899622 2017 UniProt: the universal protein knowledgebase.