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rs7576192

From SNPedia

Orientationplus
Stabilizedplus
Make rs7576192(A;A)
Make rs7576192(A;G)
Make rs7576192(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position120360455
is asnp
is mentioned by
dbSNPrs7576192
ebirs7576192
HLIrs7576192
Exacrs7576192
Varsomers7576192
Maprs7576192
PheGenIrs7576192
hapmaprs7576192
1000 genomesrs7576192
hgdprs7576192
ensemblrs7576192
gopubmedrs7576192
geneviewrs7576192
scholarrs7576192
googlers7576192
pharmgkbrs7576192
gwascentralrs7576192
openSNPrs7576192
23andMers7576192
23andMe allrs7576192
SNP Nexus

SNPshotrs7576192
SNPdbers7576192
MSV3drs7576192
GWAS Ctlgrs7576192
GMAF0.2888
Max Magnitude
? (A;A) (A;G) (G;G) 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