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rs7579169

From SNPedia

Orientationplus
Stabilizedplus
Make rs7579169(C;C)
Make rs7579169(C;T)
Make rs7579169(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position120360548
is asnp
is mentioned by
dbSNPrs7579169
ebirs7579169
HLIrs7579169
Exacrs7579169
Varsomers7579169
Maprs7579169
PheGenIrs7579169
hapmaprs7579169
1000 genomesrs7579169
hgdprs7579169
ensemblrs7579169
gopubmedrs7579169
geneviewrs7579169
scholarrs7579169
googlers7579169
pharmgkbrs7579169
gwascentralrs7579169
openSNPrs7579169
23andMers7579169
23andMe allrs7579169
SNP Nexus

SNPshotrs7579169
SNPdbers7579169
MSV3drs7579169
GWAS Ctlgrs7579169
GMAF0.2879
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22432041OA-icon.png] Genome-Wide Association Scan Identifies a Risk Locus for Preeclampsia on 2q14, Near the Inhibin, Beta B Gene


[PMID 26313529] Single nucleotide polymorphisms near the inhibin beta B gene on 2q14 are associated with pre-eclampsia in Han Chinese women


[PMID 26313396] Association of single nucleotide polymorphism rs7579169 with hypertension disorders during pregnancy and perinatal outcome


[PMID 27173354] Common variant rs7579169 is associated with preeclampsia in Han Chinese women.