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.