Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11617740
rs11617740
FGF14
0.800 GeneticVariation GWASDB Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort. 23551011

2013
dbSNP: rs11617740
rs11617740
FGF14
0.800 GeneticVariation GWASCAT Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort. 23551011

2013
dbSNP: rs2839440
rs2839440
ZNF295-AS1
0.800 GeneticVariation GWASCAT Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort. 23551011

2013
dbSNP: rs2839440
rs2839440
ZNF295-AS1
0.800 GeneticVariation GWASDB Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort. 23551011

2013
dbSNP: rs7322722
rs7322722
MYCBP2
0.800 GeneticVariation GWASCAT Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort. 23551011

2013
dbSNP: rs7322722
rs7322722
MYCBP2
0.800 GeneticVariation GWASDB Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort. 23551011

2013
dbSNP: rs12711941
rs12711941 		0.700 GeneticVariation GWASDB Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene. 22432041

2012
dbSNP: rs7576192
rs7576192 		0.700 GeneticVariation GWASDB Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene. 22432041

2012
dbSNP: rs7579169
rs7579169 		0.700 GeneticVariation GWASDB Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene. 22432041

2012
dbSNP: rs1163944538
rs1163944538
TMEM94
GA 0.700 CausalMutation CLINVAR

dbSNP: rs1352010373
rs1352010373
TMEM94
C 0.700 CausalMutation CLINVAR

dbSNP: rs137854539
rs137854539
GNAS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs137854889
rs137854889
ZMPSTE24
GT 0.700 CausalMutation CLINVAR

dbSNP: rs1555727493
rs1555727493
KMT2B
TGGCGGCGGCGGCG 0.700 CausalMutation CLINVAR

dbSNP: rs1565706229
rs1565706229
EED ; MIR6755
C 0.700 GeneticVariation CLINVAR

dbSNP: rs267607079
rs267607079
SOS1
G 0.700 CausalMutation CLINVAR

dbSNP: rs587784177
rs587784177
NSD1
A 0.700 GeneticVariation CLINVAR