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rs11600901

From SNPedia

Orientationplus
Stabilizedplus
Make rs11600901(A;A)
Make rs11600901(A;G)
Make rs11600901(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position118161271
GeneSCN2B
is asnp
is mentioned by
dbSNPrs11600901
ebirs11600901
HLIrs11600901
Exacrs11600901
Varsomers11600901
Maprs11600901
PheGenIrs11600901
hapmaprs11600901
1000 genomesrs11600901
hgdprs11600901
ensemblrs11600901
gopubmedrs11600901
geneviewrs11600901
scholarrs11600901
googlers11600901
pharmgkbrs11600901
gwascentralrs11600901
openSNPrs11600901
23andMers11600901
23andMe allrs11600901
SNP Nexus

SNPshotrs11600901
SNPdbers11600901
MSV3drs11600901
GWAS Ctlgrs11600901
GMAF0.05739
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23551011OA-icon.png]
Trait Preeclampsia
Title 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.
Risk Allele
P-val 9E-6
Odds Ratio 9.83 [3.58-27.00]