Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs431905504
rs431905504
SLC6A3
T 0.700 CausalMutation CLINVAR Genetic mapping and exome sequencing identify variants associated with five novel diseases. 22279524

2012
dbSNP: rs1303000329
rs1303000329
DLC1
A 0.700 SusceptibilityMutation CLINVAR

dbSNP: rs1206846668
rs1206846668
FOLH1
0.010 GeneticVariation BEFREE In addition, the MTHFR 677C > T variant conferred a modest protective effect in SBO mothers and the total NTD mother group, but not in SBA mothers. 14616766

2003
dbSNP: rs1217691063
rs1217691063
MTHFR
0.010 GeneticVariation BEFREE In addition, the MTHFR 677C > T variant conferred a modest protective effect in SBO mothers and the total NTD mother group, but not in SBA mothers. 14616766

2003
dbSNP: rs368087026
rs368087026
SLC19A1
0.010 GeneticVariation BEFREE In addition, the MTHFR 677C > T variant conferred a modest protective effect in SBO mothers and the total NTD mother group, but not in SBA mothers. 14616766

2003
dbSNP: rs775144154
rs775144154
SLC19A1
0.010 GeneticVariation BEFREE The RFC-1 80G > A variant elevated the risk of SBO and anencephalic pregnancy. 14616766

2003