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rs6563695

From SNPedia

Orientationplus
Stabilizedplus
Make rs6563695(G;G)
Make rs6563695(G;T)
Make rs6563695(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position39329106
is asnp
is mentioned by
dbSNPrs6563695
ebirs6563695
HLIrs6563695
Exacrs6563695
Varsomers6563695
Maprs6563695
PheGenIrs6563695
hapmaprs6563695
1000 genomesrs6563695
hgdprs6563695
ensemblrs6563695
gopubmedrs6563695
geneviewrs6563695
scholarrs6563695
googlers6563695
pharmgkbrs6563695
gwascentralrs6563695
openSNPrs6563695
23andMers6563695
23andMe allrs6563695
SNP Nexus

SNPshotrs6563695
SNPdbers6563695
MSV3drs6563695
GWAS Ctlgrs6563695
GMAF0.141
Max Magnitude
? (G;G) (G;T) (T;T) 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 5E-6
Odds Ratio 3.65 [2.09-6.36]