Condition: NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO


rs12170597 in CELSR1 gene and NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO PMID 22095531 2012 Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis.

rs778976254 in DACT1 gene and NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO PMID 22610794 2012 Identification of novel rare mutations of DACT1 in human neural tube defects.

rs1114167354 in PARD3 gene and NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO PMID 27925688 2017 Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects Via Disrupting Apical Tight Junction Formation.

rs1302482009 in SCRIB gene and NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO PMID 22095531 2012 Mutations in the planar cell polarity genes CELSR1 and SCRIB are associated with the severe neural tube defect craniorachischisis.

rs121918219 in VANGL1 gene and NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO PMID 19319979 2009 Novel mutations in VANGL1 in neural tube defects.

PMID 17409324 2007 Mutations in VANGL1 associated with neural-tube defects.

rs267607167 in VANGL2 gene and NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO PMID 20558380 2010 VANGL2 mutations in human cranial neural-tube defects.